Ndc 57844 130 01 - Generic Name,Company Name, Contact Info, Presentation, Type of Update,Date of Update, Availability Information, Related Information, Resolved Note, Reason for ...

 
The product is distributed in a single package with assigned NDC code 57844-130-01 100 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk. . Exterior semi gloss enamel paint

National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...57844-117-01, 57844-120-01, 57844-130-01 Packager: Teva Pharmaceuticals USA, Inc. ADDERALL XR (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine sulfate and amphetamine aspartate) capsule, extended release National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...NDC 42494-416-25. CIV PHENOBARBITAL Sodium Injection, USP. 130 mg/mL R x only. FOR IM OR SLOW IV USE. 25 x 1 mL Vials. Store at 20°-25°C (68°-77°F) [See USP Controlled Room Temperature] DO NOT USE IF DISCOLORED OR CONTAINS A PRECIPITATE. MANUFACTURED FOR: CAMERON PHARMACEUTICALS LLC. GTIN: 00342494416258 SN: 115000433564 EXP: 01-2030 LOT ...NDC Code(s): 57844-105-01, ... 57844-130-01 Packager: Teva Pharmaceuticals USA, Inc. ADDERALL XR (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine ...Product Details Strength 12.5 mg Package Details 100 Tablets/Bottle NDC number 57844-0112-01 View PI Product Details Strength 15 mg Package Details 100 Tablets/Bottle NDC number 57844-0115-01 View PI Product Details National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...57844-130-01 Adderall Labeler Name Teva Pharmaceuticals USA, Inc. Name of Company corresponding to the labeler code segment of the ProductNDC. NDC Package Code 57844-130-01 The labeler code, product code, and package code segments of the National Drug Code number, separated by hyphens. Asterisks are no longer used or includedThey are available in bottles of 100 tablets (NDC 57844-120-01). 30 mg: Peach, round, flat-faced beveled edge tablet with one full bisect and 2 partial bisects debossed with 3 | 0 on one side and dp on the other side. They are available in bottles of 100 tablets (NDC 57844-130-01).National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...NDC: Methylprednisolone Sodium Succinate for Injection, USP: Packaging Configuration: NDC 43598-127-25: 40 mg Single- Dose Vial: 25 vials per Carton: NDC 43598-129-25: 125 mg Single- Dose Vial: 25 vials per Carton: NDC 43598-128-11 : 500 mg Multi-Dose Vial: 1 vial per Carton: NDC 43598-130-74: 1 g Multi-Dose Vial: 1 vial per CartonNational Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... The initial dosage of Dexamethasone Sodium Phosphate Injection, USP may vary from 0.5 mg/day to 9 mg/day depending on the specific disease entity ... HOW SUPPLIED. Dexamethasone Sodium Phosphate Injection, USP is a sterile, clear, colorless solution, essentially free from visible particles and is supplied as follows: 10 mg per mL - 1 mL Single ...Buy Adderall Online Overnight | 5mg, 12.5mg, 10mg, 20mg, 30mg with 30% off has published 0 articles and reviewed 0 in The Cureus Journal of Medical Science. They are available in bottles of 100 tablets (NDC 57844-120-01). 30 mg: Peach, round, flat-faced beveled edge tablet with one full bisect and 2 partial bisects debossed with 3 | 0 on one side and dp on the other side. They are available in bottles of 100 tablets (NDC 57844-130-01). The initial dosage of Dexamethasone Sodium Phosphate Injection, USP may vary from 0.5 mg/day to 9 mg/day depending on the specific disease entity ... HOW SUPPLIED. Dexamethasone Sodium Phosphate Injection, USP is a sterile, clear, colorless solution, essentially free from visible particles and is supplied as follows: 10 mg per mL - 1 mL Single ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Aug 13, 2023 · Amphetamine mixed salts immediate release tablet, Lannett, 30 mg, bottle, 100 count, NDC 00527-1506-37. Amphetamine mixed salts immediate release tablet, Lannett, 7.5 mg, bottle, 100 count, NDC 00527-1501-37. Amphetamine mixed salts immediate release tablet, Rhodes, 10 mg, bottle, 100 count, NDC 42858-0723-01. National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... Amphetamine mixed salts immediate release tablet, Lannett, 30 mg, bottle, 100 count, NDC 00527-1506-37. Amphetamine mixed salts immediate release tablet, Lannett, 7.5 mg, bottle, 100 count, NDC 00527-1501-37. Amphetamine mixed salts immediate release tablet, Rhodes, 10 mg, bottle, 100 count, NDC 42858-0723-01.National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...In addition, Janssen CarePath can also investigate specialty pharmacies that may be available to simplify product procurement and billing for healthcare providers. If you have any questions, please call a Janssen CarePath Care Coordinator at 877-CarePath (877-227-3728), Monday-Friday, 8:00 AM to 8:00 PM ET.NDC Number: 57844-0181-13: Product Dating: McKesson Acceptable Dating: we will ship >= 180 days: Storage Requirements: USP Controlled Room Temperature: Strength: 10 ...Tablets are packaged in bottles of 30 (NDC 57844-140-56) and 100 (NDC 57844-140-01). Each capsule has an opaque white body and an opaque bright blue cap. Each capsule is imprinted with “ADIPEX-P” - “37.5” on the cap and two stripes on the body using dark blue ink. Capsules are packaged in bottles of 100 (NDC 57844-019-01).SEARCH RESULTS for: 577957 [RxCUI] (24 results) Share Adderall immediate release tablet, Teva, 5 mg, bottle, 100 count, NDC 57844-0105-01 Adderall immediate release tablet, Teva, 7.5 mg, bottle, 100 count, NDC 57844-0117-01 Amphetamine mixed salts immediate release tablet, Mallinckrodt, 10 mg, bottle, 100 count, NDC 00406-8892-01Mar 24, 2022 · NDC 47426-201-01 Rx Only. CINVANTI ® (aprepitant) injectable emulsion. 130 mg/18 mL (7.2 mg/mL) For Intravenous Use Only. Must be refrigerated. Store at 2°C-8°C (36°F-46°F). Do Not Freeze. 1 Sterile Single-Dose Vial Discard Unused Portion. Not For Sale. HERON THERAPEUTICS National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Mar 10, 2022 · 3/10/2022 Amphetamine Mixed Salts, Immediate-Release Tablets Products Affected - Description Amphetamine mixed salts immediate release tablet, Mylan, 12.5 mg, bottle, 100 count, NDC 00378-4544-01 - discontinued Amphetamine mixed salts immediate release tablet, Mylan, 15 mg, bottle, 100 count, NDC 00378-4545-01 - discontinued NDC Number: 57844013001: Product Dating: McKesson Acceptable Dating: we will ship >= 90 days: Quantity: 100 Tablets: Strength: 30 mg: UNSPSC Code: 51143801Amphetamine marketed by Teva Pharmaceuticals USA, Inc. under NDC Code 57844-130-01 NDC Code (s) : 57844-105-01, 57844-117-01, 57844-110-01, 57844-112-01, 57844-115-01, 57844-120-01, 57844-130-01 Packager : Teva Pharmaceuticals USA, Inc. Category : HUMAN PRESCRIPTION DRUG LABEL DEA Schedule : CII Marketing Status : New Drug Application 57844-130-01 Adderall Labeler Name Teva Pharmaceuticals USA, Inc. Name of Company corresponding to the labeler code segment of the ProductNDC. NDC Package Code 57844-130-01 The labeler code, product code, and package code segments of the National Drug Code number, separated by hyphens. Asterisks are no longer used or includedTeva Acknowledges Scrutiny In Adderall Shortage. That Adderall sales estimate is a drop in the bucket for Teva. The company reported $15.9 billion in 2021 sales and pulled in $14.9 billion in ...Amphetamine marketed by Teva Pharmaceuticals USA, Inc. under NDC Code 57844-130-01 NDC Code (s) : 57844-105-01, 57844-117-01, 57844-110-01, 57844-112-01, 57844-115-01, 57844-120-01, 57844-130-01 Packager : Teva Pharmaceuticals USA, Inc. Category : HUMAN PRESCRIPTION DRUG LABEL DEA Schedule : CII Marketing Status : New Drug ApplicationNational Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... CanMED: NDC. The Cancer Medications Enquiry Database (CanMED) is a two-part resource for cancer drug treatment related studies. ... (16714-130-01) / 1 mL in 1 VIAL ...NDC Code(s): 13537-450-01, ... 57844-117-01, 57844-120-01, 57844-130-01 ... 57844-130-01 Packager: TEVA PHARMACEUTICALS USA, INC. < previous | page of 50 | next > Why ... National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... SEARCH RESULTS for: 7CVR7L4A2D (1000 results) Only the first 1000 of 3471 Advanced Search results were returned, please refine your search further by modifying your query.National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Amphetamine marketed by Teva Pharmaceuticals USA, Inc. under NDC Code 57844-130-01 NDC Code (s) : 57844-105-01, 57844-117-01, 57844-110-01, 57844-112-01, 57844-115-01, 57844-120-01, 57844-130-01 Packager : Teva Pharmaceuticals USA, Inc. Category : HUMAN PRESCRIPTION DRUG LABEL DEA Schedule : CII Marketing Status : New Drug ApplicationNational Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... Code: 16714-0130-01 Description: 1 VIAL in 1 CARTON (16714-130-01) / 1 mL in 1 VIAL Effective Date: Nov. 19, 2019 They are available in bottles of 100 tablets (NDC 57844-130-01). Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...NDC: Methylprednisolone Sodium Succinate for Injection, USP: Packaging Configuration: NDC 43598-127-25: 40 mg Single- Dose Vial: 25 vials per Carton: NDC 43598-129-25: 125 mg Single- Dose Vial: 25 vials per Carton: NDC 43598-128-11 : 500 mg Multi-Dose Vial: 1 vial per Carton: NDC 43598-130-74: 1 g Multi-Dose Vial: 1 vial per CartonIn addition, Janssen CarePath can also investigate specialty pharmacies that may be available to simplify product procurement and billing for healthcare providers. If you have any questions, please call a Janssen CarePath Care Coordinator at 877-CarePath (877-227-3728), Monday-Friday, 8:00 AM to 8:00 PM ET.Feb 26, 2020 · NDC 42494-416-25. CIV PHENOBARBITAL Sodium Injection, USP. 130 mg/mL R x only. FOR IM OR SLOW IV USE. 25 x 1 mL Vials. Store at 20°-25°C (68°-77°F) [See USP Controlled Room Temperature] DO NOT USE IF DISCOLORED OR CONTAINS A PRECIPITATE. MANUFACTURED FOR: CAMERON PHARMACEUTICALS LLC. GTIN: 00342494416258 SN: 115000433564 EXP: 01-2030 LOT ... They are available in bottles of 100 tablets (NDC 57844-130-01). Store at 20° to 25°C (68° to 77°F) [See USP Controlled Room Temperature]. Dispense in a tight, light-resistant container as defined in the USP, with a child-resistant closure (as required).National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Adderall immediate release tablet, Teva, 5 mg, bottle, 100 count, NDC 57844-0105-01 Adderall immediate release tablet, Teva, 7.5 mg, bottle, 100 count, NDC 57844-0117-01 Amphetamine mixed salts immediate release tablet, Mallinckrodt, 10 mg, bottle, 100 count, NDC 00406-8892-01National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...SEARCH RESULTS for: 1009145 [RxCUI] (22 results) ShareNational Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... They are available in bottles of 100 tablets (NDC 57844-120-01). 30 mg: Peach, round, flat-faced beveled edge tablet with one full bisect and 2 partial bisects debossed with 3 | 0 on one side and dp on the other side. They are available in bottles of 100 tablets (NDC 57844-130-01). 57844-117-01, 57844-120-01, 57844-130-01 Packager: Teva Pharmaceuticals USA, Inc. ADDERALL XR (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine sulfate and amphetamine aspartate) capsule, extended release On July 22, 2022, FDA announced the availability of a proposed rule, Revising the National Drug Code Format and Drug Label Barcode Requirements (Docket No. FDA-2021-N-1351), that is intended to ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Amphetamine marketed by Teva Pharmaceuticals USA, Inc. under NDC Code 57844-130-01 NDC Code (s) : 57844-105-01, 57844-117-01, 57844-110-01, 57844-112-01, 57844-115-01, 57844-120-01, 57844-130-01 Packager : Teva Pharmaceuticals USA, Inc. Category : HUMAN PRESCRIPTION DRUG LABEL DEA Schedule : CII Marketing Status : New Drug Application National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... NDC 57844-130-01. Adderall ® CII (Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate and Amphetamine Sulfate Tablets) (Mixed Salts of a Single Entity Amphetamine Product) 30 mg. PHARMACIST: Dispense the accompanying Medication Guide to each patient. Rx only. 100 Tablets90696 130: ProQuad (VFC) MMRV: 12 months - 12 years 0.5 ml: SC ... NDC: 42515-001-01 90738 134. JE-VAX - Japanese Encephalitis Japanese Encephalitis. 12 months ... SEARCH RESULTS for: 1009145 [RxCUI] (22 results) Share May 30, 2023 · NDC 57844-105-01. Adderall ® CII ... NDC:57844-130-01: 100 TABLET in 1 BOTTLE: None: Marketing Information: Marketing Category: Application Number or Monograph Citation: NDC Code(s): 57844-105-01, ... 57844-130-01 Packager: Teva Pharmaceuticals USA, Inc. ADDERALL XR (dextroamphetamine sulfate, dextroamphetamine saccharate, amphetamine ...Buy Adderall Online Overnight | 5mg, 12.5mg, 10mg, 20mg, 30mg with 30% off has published 0 articles and reviewed 0 in The Cureus Journal of Medical Science.Dec 28, 2022 · NDC:16714-130-01. Triamcinolone acetonide injectable suspension USP, 40 mg per mL. Rx Only Northstar Rx LLC. Carton Label . PRINCIPAL DISPLAY PANEL. NDC:16714-130-25. NDC 57844-130-01 100 TABLET in 1 BOTTLE (57844-130-01) Marketing Start Date: 2014-02-06: NDC Exclude Flag: N: Sample Package? N: NDC SPL Data Element Entries. Tablets are packaged in bottles of 30 (NDC 57844-140-56) and 100 (NDC 57844-140-01). Each capsule has an opaque white body and an opaque bright blue cap. Each capsule is imprinted with “ADIPEX-P” - “37.5” on the cap and two stripes on the body using dark blue ink. Capsules are packaged in bottles of 100 (NDC 57844-019-01).Adderall immediate release tablet, Teva, 5 mg, bottle, 100 count, NDC 57844-0105-01 Adderall immediate release tablet, Teva, 7.5 mg, bottle, 100 count, NDC 57844-0117-01 Amphetamine mixed salts immediate release tablet, Mallinckrodt, 10 mg, bottle, 100 count, NDC 00406-8892-01NDC 42494-416-25. CIV PHENOBARBITAL Sodium Injection, USP. 130 mg/mL R x only. FOR IM OR SLOW IV USE. 25 x 1 mL Vials. Store at 20°-25°C (68°-77°F) [See USP Controlled Room Temperature] DO NOT USE IF DISCOLORED OR CONTAINS A PRECIPITATE. MANUFACTURED FOR: CAMERON PHARMACEUTICALS LLC. GTIN: 00342494416258 SN: 115000433564 EXP: 01-2030 LOT ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...NDC Code(s): 13537-450-01, ... 57844-117-01, 57844-120-01, 57844-130-01 ... 57844-130-01 Packager: TEVA PHARMACEUTICALS USA, INC. < previous | page of 50 | next > Why ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Manufacturer/ NDC Number CPT Code: CVX Code Combination Vaccines Pediarix (VFC) DTAP-Hep B-IPV Birth - 6 years : 0.5 ml IM: GlaxoSmithKline – SKB NDC: 58160-0811-52 90723: 110 Pentacel (VFC) DTaP-Hib-IPV Birth - 4 years: 0.5 ml IM: Sanofi Pasteur – PMC NDC: 49281-0510-05 90698: 120 Kinrix (VFC) DTaP-IPV 4 - 6 years: 0.5 ml IM ...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... Code: 16714-0130-01 Description: 1 VIAL in 1 CARTON (16714-130-01) / 1 mL in 1 VIAL Effective Date: Nov. 19, 2019 Requests for more specific information should be submitted in writing or directed to FDA's Freedom of Information Staff at: Food and Drug Administration. Freedom of Information Office, New ...NDC: Methylprednisolone Sodium Succinate for Injection, USP: Packaging Configuration: NDC 43598-127-25: 40 mg Single- Dose Vial: 25 vials per Carton: NDC 43598-129-25: 125 mg Single- Dose Vial: 25 vials per Carton: NDC 43598-128-11 : 500 mg Multi-Dose Vial: 1 vial per Carton: NDC 43598-130-74: 1 g Multi-Dose Vial: 1 vial per CartonSEARCH RESULTS for: 541878 [RxCUI] (25 results) ShareManufacturer/ NDC Number CPT Code: CVX Code Combination Vaccines Pediarix (VFC) DTAP-Hep B-IPV Birth - 6 years : 0.5 ml IM: GlaxoSmithKline – SKB NDC: 58160-0811-52 90723: 110 Pentacel (VFC) DTaP-Hib-IPV Birth - 4 years: 0.5 ml IM: Sanofi Pasteur – PMC NDC: 49281-0510-05 90698: 120 Kinrix (VFC) DTaP-IPV 4 - 6 years: 0.5 ml IM ...SEARCH RESULTS for: 687043 [RxCUI] (20 results) Sharein a 10-digit format. Proper billing of a National Drug Code (NDC) requires an 11-digit number in a 5-4-2 format. Converting National Drug Code (NDC) from a 10-digit to an 11-digit format requires a strategically placed zero, dependent upon the 10-digit format. The following table shows common 10-digit National Drug Code (NDC) formats National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...

Aug 28, 2023 · Triamcinolone acetonide injectable suspension, USP is a synthetic glucocorticoid corticosteroid with anti-inflammatory action. THIS FORMULATION IS SUITABLE FOR INTRAMUSCULAR AND INTRA-ARTICULAR USE ONLY. THIS FORMULATION IS NOT FOR INTRADERMAL INJECTION. Each mL of the sterile aqueous suspension provides 40 mg triamcinolone acetonide, with 0.66 ... . Daisies won

ndc 57844 130 01

segments of the NDC number, separated by hyphens per FDA website. o In the Open Payments application, this element corresponds to the “ National Drug Code (NDC) of Associated Covered Drug or Biological” field for PY2013 – PY2015 submissions or the “Associated Drug or Biological NDC” field for PY2016 onward submissions. • ProprietaryNameTablets are packaged in bottles of 30 (NDC 57844-140-56) and 100 (NDC 57844-140-01). Each capsule has an opaque white body and an opaque bright blue cap. Each capsule is imprinted with “ADIPEX-P” - “37.5” on the cap and two stripes on the body using dark blue ink. Capsules are packaged in bottles of 100 (NDC 57844-019-01). NDC:16714-130-01. Triamcinolone acetonide injectable suspension USP, 40 mg per mL. Rx Only Northstar Rx LLC. Carton Label . PRINCIPAL DISPLAY PANEL. NDC:16714-130-25.FDA’s National Drug Code (NDC) Directory contains information about finished drug products, unfinished drugs and compounded drug products. Finished drug products Drug establishments are...National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ... Amphetamine mixed salts immediate release tablet, Lannett, 30 mg, bottle, 100 count, NDC 00527-1506-37. Amphetamine mixed salts immediate release tablet, Lannett, 7.5 mg, bottle, 100 count, NDC 00527-1501-37. Amphetamine mixed salts immediate release tablet, Rhodes, 10 mg, bottle, 100 count, NDC 42858-0723-01.National Library of Medicine. REPORT ADVERSE EVENTS | Recalls ...Amphetamine mixed salts immediate release tablet, Lannett, 30 mg, bottle, 100 count, NDC 00527-1506-37. Amphetamine mixed salts immediate release tablet, Lannett, 7.5 mg, bottle, 100 count, NDC 00527-1501-37. Amphetamine mixed salts immediate release tablet, Rhodes, 10 mg, bottle, 100 count, NDC 42858-0723-01.Manufacturer/ NDC Number CPT Code: CVX Code Combination Vaccines Pediarix (VFC) DTAP-Hep B-IPV Birth - 6 years : 0.5 ml IM: GlaxoSmithKline – SKB NDC: 58160-0811-52 90723: 110 Pentacel (VFC) DTaP-Hib-IPV Birth - 4 years: 0.5 ml IM: Sanofi Pasteur – PMC NDC: 49281-0510-05 90698: 120 Kinrix (VFC) DTaP-IPV 4 - 6 years: 0.5 ml IM ...FDA’s National Drug Code (NDC) Directory contains information about finished drug products, unfinished drugs and compounded drug products. Finished drug products Drug establishments are...Generic Name,Company Name, Contact Info, Presentation, Type of Update,Date of Update, Availability Information, Related Information, Resolved Note, Reason for ... Manufacturer/ NDC Number CPT Code: CVX Code Quadracel™ VFC: DTaP/IPV 4 - 6 years: 0.5 ml IM: Sanofi Pasteur – PMC NDC: 49281-0562-10 (1 dose vial) 90696 130: Kinrix® VFC: DTaP/IPV 4 - 6 years: 0.5 ml IM: GlaxoSmithKline – SKB NDC: 58160-0812-11 (1 dose vial) NDC: 58160-0812-52 (1 dose T-L syringe) 90696: 130 Pediarix® VFC DTAP/HepB/IPV ...SEARCH RESULTS for: 1009145 [RxCUI] (22 results) Share Amphetamine marketed by Teva Pharmaceuticals USA, Inc. under NDC Code 57844-130-01 NDC Code (s) : 57844-105-01, 57844-117-01, 57844-110-01, 57844-112-01, 57844-115-01, 57844-120-01, 57844-130-01 Packager : Teva Pharmaceuticals USA, Inc. Category : HUMAN PRESCRIPTION DRUG LABEL DEA Schedule : CII Marketing Status : New Drug ApplicationThe NDC code 57844-130 is assigned by the FDA to the product Adderall which is a human prescription drug product labeled by Teva Pharmaceuticals Usa, Inc.. The generic name of Adderall is dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate..

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