Package 60760-819-30

Brand: zolpidem tartrate

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 60760-819-30
Digits Only 6076081930
Product NDC 60760-819
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-819-30)

Marketing

Marketing Status
Marketed Since 2024-08-28
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": "21769110-885f-a30e-e063-6394a90a207c", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854880"], "spl_set_id": ["21767f56-ce92-2b8c-e063-6394a90a8b76"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-819-30)", "package_ndc": "60760-819-30", "marketing_start_date": "20240828"}], "brand_name": "ZOLPIDEM TARTRATE", "product_id": "60760-819_21769110-885f-a30e-e063-6394a90a207c", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "60760-819", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZOLPIDEM TARTRATE", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "12.5 mg/1"}], "application_number": "ANDA078970", "marketing_category": "ANDA", "marketing_start_date": "20140411", "listing_expiration_date": "20261231"}