dextroamphetamine sulfate

Generic: dextroamphetamine sulfate

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dextroamphetamine sulfate
Generic Name dextroamphetamine sulfate
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

dextroamphetamine sulfate 20 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2352
Product ID 72162-2352_ef6e3d80-5391-42d2-b6f1-9cc8082a54e3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090533
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2021-08-06

Pharmacologic Class

Classes
central nervous system stimulant [epc] central nervous system stimulation [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622352
Hyphenated Format 72162-2352

Supplemental Identifiers

RxCUI
1535454
UNII
JJ768O327N

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name dextroamphetamine sulfate (source: ndc)
Generic Name dextroamphetamine sulfate (source: ndc)
Application Number ANDA090533 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (72162-2352-3)
source: ndc

Packages (1)

Ingredients (1)

dextroamphetamine sulfate (20 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ef6e3d80-5391-42d2-b6f1-9cc8082a54e3", "openfda": {"unii": ["JJ768O327N"], "rxcui": ["1535454"], "spl_set_id": ["b40c9a90-7e2e-48d6-adb6-2351c0ca621d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2352-3)", "package_ndc": "72162-2352-3", "marketing_start_date": "20240814"}], "brand_name": "Dextroamphetamine Sulfate", "product_id": "72162-2352_ef6e3d80-5391-42d2-b6f1-9cc8082a54e3", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-2352", "dea_schedule": "CII", "generic_name": "Dextroamphetamine Sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dextroamphetamine Sulfate", "active_ingredients": [{"name": "DEXTROAMPHETAMINE SULFATE", "strength": "20 mg/1"}], "application_number": "ANDA090533", "marketing_category": "ANDA", "marketing_start_date": "20210806", "listing_expiration_date": "20261231"}