Package 67046-1594-3

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1594-3
Digits Only 6704615943
Product NDC 67046-1594
Product ID 67046-1594_3eeee505-7359-01ee-e063-6294a90ae5e3
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1594-3)

Marketing

Marketing Status
Marketed Since 2025-09-16
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": "3eeee505-7359-01ee-e063-6294a90ae5e3", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["3eeee3b7-188a-05a0-e063-6294a90a1853"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1594-3)", "package_ndc": "67046-1594-3", "marketing_start_date": "20250916"}], "brand_name": "Metformin Hydrochloride", "product_id": "67046-1594_3eeee505-7359-01ee-e063-6294a90ae5e3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "67046-1594", "generic_name": "Metformin Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA209882", "marketing_category": "ANDA", "marketing_start_date": "20250916", "listing_expiration_date": "20261231"}