Package 17224-970-30

Brand: zolpidem tartrate

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 17224-970-30
Digits Only 1722497030
Product NDC 17224-970
Description

30 TABLET in 1 BOTTLE (17224-970-30)

Marketing

Marketing Status
Marketed Since 2007-09-05
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": "4873895f-0366-4dd3-e063-6294a90a10c8", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["7da75d2b-905c-4fdf-bc53-1358c6477755"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (17224-970-30)", "package_ndc": "17224-970-30", "marketing_start_date": "20070905"}], "brand_name": "ZOLPIDEM TARTRATE", "product_id": "17224-970_4873895f-0366-4dd3-e063-6294a90a10c8", "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": "17224-970", "dea_schedule": "CIV", "generic_name": "ZOLPIDEM TARTRATE", "labeler_name": "Calvin Scott & Co., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZOLPIDEM TARTRATE", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA077903", "marketing_category": "ANDA", "marketing_start_date": "20070905", "listing_expiration_date": "20271231"}