Package 68071-3770-9

Brand: zolpidem tartrate

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 68071-3770-9
Digits Only 6807137709
Product NDC 68071-3770
Description

90 TABLET, FILM COATED in 1 BOTTLE (68071-3770-9)

Marketing

Marketing Status
Marketed Since 2025-01-13
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": "2b9f78c9-0a32-f12c-e063-6294a90ae129", "openfda": {"upc": ["0368071377095"], "unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["2b9f696a-b637-4dea-e063-6394a90aeb2e"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3770-9)", "package_ndc": "68071-3770-9", "marketing_start_date": "20250113"}], "brand_name": "Zolpidem Tartrate", "product_id": "68071-3770_2b9f78c9-0a32-f12c-e063-6294a90ae129", "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": "68071-3770", "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": "10 mg/1"}], "application_number": "ANDA078413", "marketing_category": "ANDA", "marketing_start_date": "20070504", "listing_expiration_date": "20261231"}