Package 80425-0060-1

Brand: zolpidem tartrate

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 80425-0060-1
Digits Only 8042500601
Product NDC 80425-0060
Product ID 80425-0060_2a98ebb7-ca47-d2dd-e063-6294a90ac15c
Description

30 TABLET, COATED in 1 BOTTLE (80425-0060-1)

Marketing

Marketing Status
Marketed Since 2007-04-23
Brand zolpidem tartrate
Generic zolpidem tartrate
Sample Package No

Linked Drug Pages (1)

Zolpidem Tartrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a98ebb7-ca47-d2dd-e063-6294a90ac15c", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["af87b722-cdb7-0b17-e053-2a95a90a315b"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (80425-0060-1)", "package_ndc": "80425-0060-1", "marketing_start_date": "20070423"}], "brand_name": "Zolpidem Tartrate", "product_id": "80425-0060_2a98ebb7-ca47-d2dd-e063-6294a90ac15c", "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": "80425-0060", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "Advanced Rx of Tennessee, 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": "20070423", "listing_expiration_date": "20261231"}