Package 0024-5421-31

Brand: ambien

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 0024-5421-31
Digits Only 0024542131
Product NDC 0024-5421
Description

100 TABLET, FILM COATED in 1 BOTTLE (0024-5421-31)

Marketing

Marketing Status
Discontinued 2026-09-30
Brand ambien
Generic zolpidem tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3d6feaca-4f30-4ca9-a9c8-d9038744fa2f", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873", "854875", "854876", "854878"], "spl_set_id": ["c36cadf4-65a4-4466-b409-c82020b42452"], "manufacturer_name": ["Sanofi-Aventis U.S. LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0024-5421-31)", "package_ndc": "0024-5421-31", "marketing_end_date": "20260930", "marketing_start_date": "19930401"}], "brand_name": "Ambien", "product_id": "0024-5421_3d6feaca-4f30-4ca9-a9c8-d9038744fa2f", "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": "0024-5421", "dea_schedule": "CIV", "generic_name": "zolpidem tartrate", "labeler_name": "Sanofi-Aventis U.S. LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ambien", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "10 mg/1"}], "application_number": "NDA019908", "marketing_category": "NDA", "marketing_end_date": "20260930", "marketing_start_date": "19930401"}