Package 82868-064-30
Brand: zolpidem tartrate
Generic: zolpidem tartratePackage Facts
Identity
Package NDC
82868-064-30
Digits Only
8286806430
Product NDC
82868-064
Description
30 TABLET in 1 BOTTLE, PLASTIC (82868-064-30)
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": "46dccd28-a51e-7582-e063-6294a90ad34a", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["26e20f53-c042-eac0-e063-6394a90acfca"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (82868-064-30)", "package_ndc": "82868-064-30", "marketing_start_date": "20240801"}], "brand_name": "ZOLPIDEM TARTRATE", "product_id": "82868-064_46dccd28-a51e-7582-e063-6294a90ad34a", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "82868-064", "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": "ANDA077903", "marketing_category": "ANDA", "marketing_start_date": "20240801", "listing_expiration_date": "20261231"}