amphetamine sulfate

Generic: amphetamine sulfate

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

Drug Facts

Product Profile

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

amphetamine sulfate 10 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2990
Product ID 71335-2990_ff1c5297-0a96-42c0-9c9c-9fc9c7165b5f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212901
DEA Schedule cii
Listing Expiration 2027-12-31
Marketing Start 2020-05-25

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 713352990
Hyphenated Format 71335-2990

Supplemental Identifiers

RxCUI
1600695
UNII
6DPV8NK46S

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 amphetamine sulfate (source: ndc)
Generic Name amphetamine sulfate (source: ndc)
Application Number ANDA212901 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 120 TABLET in 1 BOTTLE (71335-2990-1)
source: ndc

Packages (1)

71335-2990-1 120 TABLET in 1 BOTTLE (71335-2990-1)

Ingredients (1)

amphetamine sulfate (10 mg/1)

Linked Drug Pages (1)

AMPHETAMINE SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ff1c5297-0a96-42c0-9c9c-9fc9c7165b5f", "openfda": {"unii": ["6DPV8NK46S"], "rxcui": ["1600695"], "spl_set_id": ["9817a519-fdb0-474a-92f4-2e485c9cb047"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-2990-1)", "package_ndc": "71335-2990-1", "marketing_start_date": "20260204"}], "brand_name": "AMPHETAMINE SULFATE", "product_id": "71335-2990_ff1c5297-0a96-42c0-9c9c-9fc9c7165b5f", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "71335-2990", "dea_schedule": "CII", "generic_name": "amphetamine sulfate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AMPHETAMINE SULFATE", "active_ingredients": [{"name": "AMPHETAMINE SULFATE", "strength": "10 mg/1"}], "application_number": "ANDA212901", "marketing_category": "ANDA", "marketing_start_date": "20200525", "listing_expiration_date": "20271231"}