Package 72189-658-30

Brand: metformin hcl

Generic: metformin hcl
NDC Package

Package Facts

Identity

Package NDC 72189-658-30
Digits Only 7218965830
Product NDC 72189-658
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-658-30)

Marketing

Marketing Status
Marketed Since 2026-01-29
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": "49ee8e39-a478-065d-e063-6394a90ae127", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["498ac5fc-14be-d36a-e063-6394a90a3012"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-658-30)", "package_ndc": "72189-658-30", "marketing_start_date": "20260129"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (72189-658-82)", "package_ndc": "72189-658-82", "marketing_start_date": "20260129"}], "brand_name": "Metformin HCL", "product_id": "72189-658_49ee8e39-a478-065d-e063-6394a90ae127", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "72189-658", "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": "ANDA209882", "marketing_category": "ANDA", "marketing_start_date": "20260129", "listing_expiration_date": "20271231"}