Package 82009-117-10

Brand: metformin er 500 mg

Generic: metformin er 500 mg
NDC Package

Package Facts

Identity

Package NDC 82009-117-10
Digits Only 8200911710
Product NDC 82009-117
Description

1000 TABLET in 1 BOTTLE (82009-117-10)

Marketing

Marketing Status
Marketed Since 2023-07-25
Brand metformin er 500 mg
Generic metformin er 500 mg
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "451e9a75-128c-6b1d-e063-6394a90aa5d8", "openfda": {"upc": ["0382009117102", "0382009118017"], "unii": ["786Z46389E"], "rxcui": ["860975", "860981"], "spl_set_id": ["ff196435-14f4-8b9d-e053-6294a90a4ee8"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (82009-117-10)", "package_ndc": "82009-117-10", "marketing_start_date": "20230725"}], "brand_name": "Metformin ER 500 mg", "product_id": "82009-117_451e9a75-128c-6b1d-e063-6394a90aa5d8", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "82009-117", "generic_name": "Metformin ER 500 mg", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin ER 500 mg", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA209313", "marketing_category": "ANDA", "marketing_start_date": "20230725", "listing_expiration_date": "20261231"}