Package 63629-1170-1

Brand: zolpidem

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 63629-1170-1
Digits Only 6362911701
Product NDC 63629-1170
Description

100 TABLET in 1 BOTTLE (63629-1170-1)

Marketing

Marketing Status
Marketed Since 2020-09-24
Brand zolpidem
Generic zolpidem tartrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "c6881377-aff2-41d1-9c4d-29a3d094e0a5", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854876"], "spl_set_id": ["fff2e7fc-2f7e-43c9-bfb3-d929ecc9eb72"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-1170-1)", "package_ndc": "63629-1170-1", "marketing_start_date": "20200924"}], "brand_name": "Zolpidem", "product_id": "63629-1170_c6881377-aff2-41d1-9c4d-29a3d094e0a5", "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": "63629-1170", "dea_schedule": "CIV", "generic_name": "Zolpidem Tartrate", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zolpidem", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA077214", "marketing_category": "ANDA", "marketing_start_date": "20200924", "listing_expiration_date": "20261231"}