Package 69367-412-60

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-412-60
Digits Only 6936741260
Product NDC 69367-412
Product ID 69367-412_0bcfb466-d20c-472a-8e3e-aee3df526272
Description

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69367-412-60)

Marketing

Marketing Status
Marketed Since 2025-10-23
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": "0bcfb466-d20c-472a-8e3e-aee3df526272", "openfda": {"upc": ["0369367412605", "0369367413602"], "unii": ["786Z46389E"], "rxcui": ["1807894", "1807917"], "spl_set_id": ["07b4ee2a-8435-4d38-a6b0-b919e3424153"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69367-412-60)", "package_ndc": "69367-412-60", "marketing_start_date": "20251023"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "69367-412_0bcfb466-d20c-472a-8e3e-aee3df526272", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "69367-412", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203832", "marketing_category": "ANDA", "marketing_start_date": "20251023", "listing_expiration_date": "20261231"}