Package 71335-2990-1

Brand: amphetamine sulfate

Generic: amphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 71335-2990-1
Digits Only 7133529901
Product NDC 71335-2990
Product ID 71335-2990_ff1c5297-0a96-42c0-9c9c-9fc9c7165b5f
Description

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

Marketing

Marketing Status
Marketed Since 2026-02-04
Brand amphetamine sulfate
Generic amphetamine sulfate
Sample Package No

Linked Drug Pages (1)

AMPHETAMINE SULFATE ndc-match (0.95)

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"}