Package 71335-2303-1

Brand: zolpidem

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 71335-2303-1
Digits Only 7133523031
Product NDC 71335-2303
Description

1000 TABLET in 1 BOTTLE (71335-2303-1)

Marketing

Marketing Status
Marketed Since 2023-12-01
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": "63c2f4f7-4863-463b-be0e-5ac58f64f9c5", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["33094305-4bbd-4b52-9079-8853d5f83682"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (71335-2303-1)", "package_ndc": "71335-2303-1", "marketing_start_date": "20231201"}], "brand_name": "Zolpidem", "product_id": "71335-2303_63c2f4f7-4863-463b-be0e-5ac58f64f9c5", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Agonists [MoA]", "Pyridines [CS]", "gamma-Aminobutyric Acid-ergic Agonist [EPC]"], "product_ndc": "71335-2303", "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": "10 mg/1"}], "application_number": "ANDA077214", "marketing_category": "ANDA", "marketing_start_date": "20200924", "listing_expiration_date": "20261231"}