Package 68071-3531-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3531-1
Digits Only 6807135311
Product NDC 68071-3531
Description

100 TABLET in 1 BOTTLE (68071-3531-1)

Marketing

Marketing Status
Marketed Since 2023-11-28
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": "2d3f9c43-31df-2883-e063-6294a90a7742", "openfda": {"upc": ["0368071353112"], "unii": ["786Z46389E"], "rxcui": ["861010"], "spl_set_id": ["0b3d5420-d60c-8385-e063-6394a90abb6c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3531-1)", "package_ndc": "68071-3531-1", "marketing_start_date": "20231128"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "68071-3531_2d3f9c43-31df-2883-e063-6294a90a7742", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68071-3531", "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"}