Package 72162-1983-1

Brand: zolpidem

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 72162-1983-1
Digits Only 7216219831
Product NDC 72162-1983
Product ID 72162-1983_1e5b61b6-a5bd-4f09-9d34-905ce32f1899
Description

100 TABLET in 1 BOTTLE (72162-1983-1)

Marketing

Marketing Status
Marketed Since 2024-04-03
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": "1e5b61b6-a5bd-4f09-9d34-905ce32f1899", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["1e5b61b6-a5bd-4f09-9d34-905ce32f1899"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1983-1)", "package_ndc": "72162-1983-1", "marketing_start_date": "20240403"}], "brand_name": "Zolpidem", "product_id": "72162-1983_1e5b61b6-a5bd-4f09-9d34-905ce32f1899", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "72162-1983", "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": "10 mg/1"}], "application_number": "ANDA077214", "marketing_category": "ANDA", "marketing_start_date": "20200924", "listing_expiration_date": "20261231"}