Package 82009-174-10

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82009-174-10
Digits Only 8200917410
Product NDC 82009-174
Product ID 82009-174_42cb62ed-35dd-431a-82b7-89d17b0f26af
Description

1000 TABLET, FILM COATED in 1 BOTTLE (82009-174-10)

Marketing

Marketing Status
Marketed Since 2025-07-18
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": "42cb62ed-35dd-431a-82b7-89d17b0f26af", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004", "861007"], "spl_set_id": ["25be863d-490c-47f6-9ad3-c828dc43fbf0"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (82009-174-10)", "package_ndc": "82009-174-10", "marketing_start_date": "20250718"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "82009-174_42cb62ed-35dd-431a-82b7-89d17b0f26af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "82009-174", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA203686", "marketing_category": "ANDA", "marketing_start_date": "20250718", "listing_expiration_date": "20261231"}