Package 72162-1369-1

Brand: amphetamine sulfate

Generic: amphetamine sulfate
NDC Package

Package Facts

Identity

Package NDC 72162-1369-1
Digits Only 7216213691
Product NDC 72162-1369
Description

100 TABLET in 1 BOTTLE (72162-1369-1)

Marketing

Marketing Status
Marketed Since 2024-01-25
Brand amphetamine sulfate
Generic amphetamine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b7799b14-8dd8-472b-8279-5f6ba27aa313", "openfda": {"unii": ["6DPV8NK46S"], "rxcui": ["1600695"], "spl_set_id": ["7f16dd18-bf30-41ef-8981-932da5df0951"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1369-1)", "package_ndc": "72162-1369-1", "marketing_start_date": "20240125"}], "brand_name": "AMPHETAMINE SULFATE", "product_id": "72162-1369_b7799b14-8dd8-472b-8279-5f6ba27aa313", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "72162-1369", "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": "ANDA211861", "marketing_category": "ANDA", "marketing_start_date": "20200402", "listing_expiration_date": "20261231"}