Package 72162-1982-1

Brand: zolpidem

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 72162-1982-1
Digits Only 7216219821
Product NDC 72162-1982
Product ID 72162-1982_2ff1da74-bb60-4476-a2c4-088373b8f83b
Description

100 TABLET in 1 BOTTLE (72162-1982-1)

Marketing

Marketing Status
Marketed Since 2023-12-05
Brand zolpidem
Generic zolpidem tartrate
Sample Package No

Linked Drug Pages (1)

Zolpidem ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2ff1da74-bb60-4476-a2c4-088373b8f83b", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854876"], "spl_set_id": ["df130798-1458-455b-a4e1-c33c4ecee43b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1982-1)", "package_ndc": "72162-1982-1", "marketing_start_date": "20231205"}], "brand_name": "Zolpidem", "product_id": "72162-1982_2ff1da74-bb60-4476-a2c4-088373b8f83b", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Agonists [MoA]", "Pyridines [CS]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "72162-1982", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA077214", "marketing_category": "ANDA", "marketing_start_date": "20200924", "listing_expiration_date": "20261231"}