Package 67046-1556-3

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1556-3
Digits Only 6704615563
Product NDC 67046-1556
Product ID 67046-1556_33ec8828-24ea-8757-e063-6394a90ae222
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1556-3)

Marketing

Marketing Status
Marketed Since 2025-04-29
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": "33ec8828-24ea-8757-e063-6394a90ae222", "openfda": {"unii": ["786Z46389E"], "rxcui": ["860981"], "spl_set_id": ["33ec9f6e-16d9-40ba-e063-6294a90ae87b"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1556-3)", "package_ndc": "67046-1556-3", "marketing_start_date": "20250429"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "67046-1556_33ec8828-24ea-8757-e063-6394a90ae222", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "67046-1556", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA217631", "marketing_category": "ANDA", "marketing_start_date": "20250429", "listing_expiration_date": "20261231"}