Package 68071-3482-2

Brand: zolpidem tartrate

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 68071-3482-2
Digits Only 6807134822
Product NDC 68071-3482
Description

2 TABLET, FILM COATED in 1 BOTTLE (68071-3482-2)

Marketing

Marketing Status
Marketed Since 2023-08-17
Brand zolpidem tartrate
Generic zolpidem tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2ad45778-ef3b-9f3e-e063-6394a90a5255", "openfda": {"upc": ["0368071348224"], "unii": ["WY6W63843K"], "rxcui": ["854876"], "spl_set_id": ["03207c75-f680-c18a-e063-6294a90afaa1"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (68071-3482-2)", "package_ndc": "68071-3482-2", "marketing_start_date": "20230817"}], "brand_name": "Zolpidem Tartrate", "product_id": "68071-3482_2ad45778-ef3b-9f3e-e063-6394a90a5255", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "68071-3482", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem Tartrate", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA078413", "marketing_category": "ANDA", "marketing_start_date": "20070504", "listing_expiration_date": "20261231"}