Package 70518-2917-1

Brand: zolpidem tartrate

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 70518-2917-1
Digits Only 7051829171
Product NDC 70518-2917
Description

30 TABLET in 1 BOTTLE, PLASTIC (70518-2917-1)

Marketing

Marketing Status
Marketed Since 2025-06-16
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": "4ab8be78-6584-7397-e063-6394a90a08db", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854876"], "spl_set_id": ["2abdcf77-d3ed-42bc-acd9-545aab75d567"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (70518-2917-1)", "package_ndc": "70518-2917-1", "marketing_start_date": "20250616"}], "brand_name": "ZOLPIDEM TARTRATE", "product_id": "70518-2917_4ab8be78-6584-7397-e063-6394a90a08db", "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": "70518-2917", "dea_schedule": "CIV", "generic_name": "zolpidem tartrate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ZOLPIDEM TARTRATE", "active_ingredients": [{"name": "ZOLPIDEM TARTRATE", "strength": "5 mg/1"}], "application_number": "ANDA077903", "marketing_category": "ANDA", "marketing_start_date": "20190926", "listing_expiration_date": "20271231"}