Package 70518-1951-2

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1951-2
Digits Only 7051819512
Product NDC 70518-1951
Product ID 70518-1951_498a95ea-832f-a15d-e063-6394a90a7026
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1951-2)

Marketing

Marketing Status
Marketed Since 2025-06-01
Brand metformin hydrochloride
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (1)

Metformin Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "498a95ea-832f-a15d-e063-6394a90a7026", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["13235d8e-ac3a-45b4-9c5d-9a9012951dfe"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1951-2)", "package_ndc": "70518-1951-2", "marketing_start_date": "20250601"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1951-3)", "package_ndc": "70518-1951-3", "marketing_start_date": "20251028"}], "brand_name": "Metformin Hydrochloride", "product_id": "70518-1951_498a95ea-832f-a15d-e063-6394a90a7026", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70518-1951", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203769", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20271231"}