Package 72189-617-30

Brand: metformin hcl

Generic: metformin hcl
NDC Package

Package Facts

Identity

Package NDC 72189-617-30
Digits Only 7218961730
Product NDC 72189-617
Description

30 TABLET in 1 BOTTLE (72189-617-30)

Marketing

Marketing Status
Marketed Since 2025-03-10
Brand metformin hcl
Generic metformin hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3ac48670-745a-c14e-e063-6294a90abe63", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["2ffeb25a-76a9-01e6-e063-6394a90ae332"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (72189-617-30)", "package_ndc": "72189-617-30", "marketing_start_date": "20250310"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (72189-617-82)", "package_ndc": "72189-617-82", "marketing_start_date": "20250310"}], "brand_name": "Metformin HCL", "product_id": "72189-617_3ac48670-745a-c14e-e063-6294a90abe63", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72189-617", "generic_name": "Metformin HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin HCL", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_start_date": "20250310", "listing_expiration_date": "20261231"}