Package 50090-7434-0

Brand: zolpidem tartrate

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 50090-7434-0
Digits Only 5009074340
Product NDC 50090-7434
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7434-0)

Marketing

Marketing Status
Marketed Since 2024-11-05
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": "b7d33bdb-759b-4905-aaaf-7723629c3fc2", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854876"], "spl_set_id": ["3ba3c29f-3835-4f4f-a39f-56fb42686f5b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7434-0)", "package_ndc": "50090-7434-0", "marketing_start_date": "20241105"}], "brand_name": "Zolpidem Tartrate", "product_id": "50090-7434_b7d33bdb-759b-4905-aaaf-7723629c3fc2", "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": "50090-7434", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "A-S Medication Solutions", "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"}