Package 68071-3575-8

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3575-8
Digits Only 6807135758
Product NDC 68071-3575
Description

180 TABLET in 1 BOTTLE (68071-3575-8)

Marketing

Marketing Status
Marketed Since 2024-02-16
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": "1182bf6f-b702-a084-e063-6394a90ae42e", "openfda": {"upc": ["0368071357585"], "unii": ["786Z46389E"], "rxcui": ["861010"], "spl_set_id": ["1182bf60-3578-a0ed-e063-6394a90aa50f"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE (68071-3575-8)", "package_ndc": "68071-3575-8", "marketing_start_date": "20240216"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "68071-3575_1182bf6f-b702-a084-e063-6394a90ae42e", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68071-3575", "generic_name": "metformin hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_start_date": "20230119", "listing_expiration_date": "20261231"}