Package 72162-1613-3

Brand: amphetamine sulfate

Generic: amphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 72162-1613-3
Digits Only 7216216133
Product NDC 72162-1613
Product ID 72162-1613_2694e3cd-8e20-481e-a59b-9003d0a72d4b
Description

30 TABLET in 1 BOTTLE (72162-1613-3)

Marketing

Marketing Status
Marketed Since 2024-07-01
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": "2694e3cd-8e20-481e-a59b-9003d0a72d4b", "openfda": {"unii": ["6DPV8NK46S"], "rxcui": ["1600695"], "spl_set_id": ["b94e2562-fd19-455f-ac10-2cc24302d27a"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-1613-3)", "package_ndc": "72162-1613-3", "marketing_start_date": "20240701"}], "brand_name": "Amphetamine Sulfate", "product_id": "72162-1613_2694e3cd-8e20-481e-a59b-9003d0a72d4b", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1613", "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": "ANDA200166", "marketing_category": "ANDA", "marketing_start_date": "20180329", "listing_expiration_date": "20261231"}