Package 63629-9613-1

Brand: zolpidem

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 63629-9613-1
Digits Only 6362996131
Product NDC 63629-9613
Description

1000 TABLET in 1 BOTTLE (63629-9613-1)

Marketing

Marketing Status
Marketed Since 2023-02-03
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": "e5e05dd8-d19e-4562-9ea1-f02b02ea6407", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854876"], "spl_set_id": ["70d7cfc3-7e54-4cd8-8911-7cf115d5c820"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (63629-9613-1)", "package_ndc": "63629-9613-1", "marketing_start_date": "20230203"}], "brand_name": "Zolpidem", "product_id": "63629-9613_e5e05dd8-d19e-4562-9ea1-f02b02ea6407", "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": "63629-9613", "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"}