Package 50090-3878-0
Brand: zolpidem tartrate
Generic: zolpidem tartratePackage Facts
Identity
Package NDC
50090-3878-0
Digits Only
5009038780
Product NDC
50090-3878
Description
10 TABLET, FILM COATED in 1 BOTTLE (50090-3878-0)
Marketing
Marketing Status
Brand
zolpidem tartrate
Generic
zolpidem tartrate
Sample Package
No
Linked Drug Pages (0)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f0422eb4-b8c1-410e-9a32-4538f743ff92", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["ef72eb73-d058-4ca3-9013-691aae8426fb"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (50090-3878-0)", "package_ndc": "50090-3878-0", "marketing_start_date": "20181128"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-3878-1)", "package_ndc": "50090-3878-1", "marketing_start_date": "20181128"}], "brand_name": "Zolpidem Tartrate", "product_id": "50090-3878_f0422eb4-b8c1-410e-9a32-4538f743ff92", "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": "50090-3878", "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": "10 mg/1"}], "application_number": "ANDA078413", "marketing_category": "ANDA", "marketing_start_date": "20070504", "listing_expiration_date": "20261231"}