Package 82868-078-30
Brand: zolpidem tartrate
Generic: zolpidem tartratePackage Facts
Identity
Package NDC
82868-078-30
Digits Only
8286807830
Product NDC
82868-078
Description
30 TABLET, COATED in 1 BOTTLE, PLASTIC (82868-078-30)
Marketing
Marketing Status
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": "47212210-9e3a-98a8-e063-6294a90a8e36", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["47212207-52a1-938b-e063-6294a90abca8"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (82868-078-30)", "package_ndc": "82868-078-30", "marketing_start_date": "20250520"}], "brand_name": "Zolpidem Tartrate", "product_id": "82868-078_47212210-9e3a-98a8-e063-6294a90a8e36", "dosage_form": "TABLET, COATED", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "82868-078", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem Tartrate", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA077322", "marketing_category": "ANDA", "marketing_start_date": "20250520", "listing_expiration_date": "20261231"}