Package 68071-3526-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3526-1
Digits Only 6807135261
Product NDC 68071-3526
Description

100 TABLET in 1 BOTTLE (68071-3526-1)

Marketing

Marketing Status
Marketed Since 2023-10-23
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": "2d3f923b-0c50-0cec-e063-6294a90ae8fa", "openfda": {"upc": ["0368071352610"], "unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["0865f83f-0f34-0690-e063-6294a90abf04"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3526-1)", "package_ndc": "68071-3526-1", "marketing_start_date": "20231023"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "68071-3526_2d3f923b-0c50-0cec-e063-6294a90ae8fa", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68071-3526", "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": "1000 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_start_date": "20230119", "listing_expiration_date": "20261231"}