Package 82009-118-01
Brand: metformin er 750 mg
Generic: metformin er 750 mgPackage Facts
Identity
Package NDC
82009-118-01
Digits Only
8200911801
Product NDC
82009-118
Description
100 TABLET in 1 BOTTLE (82009-118-01)
Marketing
Marketing Status
Brand
metformin er 750 mg
Generic
metformin er 750 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": "100 TABLET in 1 BOTTLE (82009-118-01)", "package_ndc": "82009-118-01", "marketing_start_date": "20230725"}], "brand_name": "Metformin ER 750 mg", "product_id": "82009-118_451e9a75-128c-6b1d-e063-6394a90aa5d8", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "82009-118", "generic_name": "Metformin ER 750 mg", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin ER 750 mg", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "750 mg/1"}], "application_number": "ANDA209313", "marketing_category": "ANDA", "marketing_start_date": "20230725", "listing_expiration_date": "20261231"}