Package 70518-4163-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4163-0
Digits Only 7051841630
Product NDC 70518-4163
Product ID 70518-4163_3fb7a539-66c9-490c-e063-6394a90a6701
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4163-0)

Marketing

Marketing Status
Marketed Since 2024-08-18
Brand metformin hydrochloride
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3fb7a539-66c9-490c-e063-6394a90a6701", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["c568d49f-c040-4f1e-ad36-77b05ab659c3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4163-0)", "package_ndc": "70518-4163-0", "marketing_start_date": "20240818"}], "brand_name": "Metformin Hydrochloride", "product_id": "70518-4163_3fb7a539-66c9-490c-e063-6394a90a6701", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70518-4163", "generic_name": "Metformin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA078321", "marketing_category": "ANDA", "marketing_start_date": "20240818", "listing_expiration_date": "20261231"}