Package 67046-1554-3

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1554-3
Digits Only 6704615543
Product NDC 67046-1554
Product ID 67046-1554_32ff4103-c2ac-d83a-e063-6394a90a97cc
Description

30 TABLET, COATED in 1 BLISTER PACK (67046-1554-3)

Marketing

Marketing Status
Marketed Since 2025-04-17
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": "32ff4103-c2ac-d83a-e063-6394a90a97cc", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["32ff33ed-89ed-c391-e063-6294a90ae414"], "manufacturer_name": ["Coupler, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BLISTER PACK (67046-1554-3)", "package_ndc": "67046-1554-3", "marketing_start_date": "20250417"}], "brand_name": "Metformin Hydrochloride", "product_id": "67046-1554_32ff4103-c2ac-d83a-e063-6394a90a97cc", "dosage_form": "TABLET, COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "67046-1554", "generic_name": "Metformin Hydrochloride", "labeler_name": "Coupler, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA205096", "marketing_category": "ANDA", "marketing_start_date": "20250417", "listing_expiration_date": "20261231"}