Package 70518-4262-0

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4262-0
Digits Only 7051842620
Product NDC 70518-4262
Product ID 70518-4262_4009764a-70ca-1fc1-e063-6394a90ac18e
Description

180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4262-0)

Marketing

Marketing Status
Marketed Since 2025-01-23
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": "4009764a-70ca-1fc1-e063-6394a90ac18e", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["bfd6ec0f-8264-4877-aa6d-f347f53bc426"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4262-0)", "package_ndc": "70518-4262-0", "marketing_start_date": "20250123"}], "brand_name": "Metformin Hydrochloride", "product_id": "70518-4262_4009764a-70ca-1fc1-e063-6394a90ac18e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70518-4262", "generic_name": "Metformin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA209882", "marketing_category": "ANDA", "marketing_start_date": "20250123", "listing_expiration_date": "20261231"}