Package 82009-047-10

Brand: metformin hydrochloride

Generic: metformin hydrochloride tablet
NDC Package

Package Facts

Identity

Package NDC 82009-047-10
Digits Only 8200904710
Product NDC 82009-047
Product ID 82009-047_451e8dd3-039f-4756-e063-6394a90a0483
Description

1000 TABLET in 1 BOTTLE (82009-047-10)

Marketing

Marketing Status
Marketed Since 2023-02-01
Brand metformin hydrochloride
Generic metformin hydrochloride tablet
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": "451e8dd3-039f-4756-e063-6394a90a0483", "openfda": {"upc": ["0382009046105", "0382009047102"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007"], "spl_set_id": ["f39ee08d-73db-71b9-e053-2995a90a877c"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (82009-047-10)", "package_ndc": "82009-047-10", "marketing_start_date": "20230201"}], "brand_name": "Metformin Hydrochloride", "product_id": "82009-047_451e8dd3-039f-4756-e063-6394a90a0483", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "82009-047", "generic_name": "Metformin Hydrochloride Tablet", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA090564", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20261231"}