Package 70518-3739-0

Brand: zolpidem tartrate

Generic: zolpidem tartrate
NDC Package

Package Facts

Identity

Package NDC 70518-3739-0
Digits Only 7051837390
Product NDC 70518-3739
Product ID 70518-3739_3b14fa68-13a6-cf97-e063-6394a90ad85a
Description

30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3739-0)

Marketing

Marketing Status
Marketed Since 2023-05-31
Brand zolpidem tartrate
Generic zolpidem tartrate
Sample Package No

Linked Drug Pages (1)

Zolpidem Tartrate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3b14fa68-13a6-cf97-e063-6394a90ad85a", "openfda": {"unii": ["WY6W63843K"], "rxcui": ["854873"], "spl_set_id": ["0f8488f3-851d-4111-af23-60f420aad0d6"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3739-0)", "package_ndc": "70518-3739-0", "marketing_start_date": "20230531"}], "brand_name": "Zolpidem Tartrate", "product_id": "70518-3739_3b14fa68-13a6-cf97-e063-6394a90ad85a", "dosage_form": "TABLET, COATED", "pharm_class": ["Central Nervous System Depression [PE]", "GABA A Receptor Positive Modulators [MoA]", "gamma-Aminobutyric Acid A Receptor Positive Modulator [EPC]"], "product_ndc": "70518-3739", "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": "10 mg/1"}], "application_number": "ANDA077322", "marketing_category": "ANDA", "marketing_start_date": "20230531", "listing_expiration_date": "20261231"}