Package 83301-0009-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 83301-0009-1
Digits Only 8330100091
Product NDC 83301-0009
Description

100 TABLET, COATED in 1 BOTTLE (83301-0009-1)

Marketing

Marketing Status
Marketed Since 2024-01-01
Brand metformin hydrochloride
Generic metformin hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "423f5f82-8524-65aa-e063-6294a90a1180", "openfda": {"upc": ["0383301001014", "0383301000826", "0383301000925"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["082b4de9-e452-fe71-e063-6394a90ac863"], "manufacturer_name": ["Mullan Pharmaceutical Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (83301-0009-1)", "package_ndc": "83301-0009-1", "marketing_start_date": "20240101"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (83301-0009-2)", "package_ndc": "83301-0009-2", "marketing_start_date": "20240101"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (83301-0009-3)", "package_ndc": "83301-0009-3", "marketing_start_date": "20240101"}], "brand_name": "Metformin Hydrochloride", "product_id": "83301-0009_423f5f82-8524-65aa-e063-6294a90a1180", "dosage_form": "TABLET, COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "83301-0009", "generic_name": "Metformin Hydrochloride", "labeler_name": "Mullan Pharmaceutical Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA205096", "marketing_category": "ANDA", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}