Package 68071-3739-1

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-3739-1
Digits Only 6807137391
Product NDC 68071-3739
Product ID 68071-3739_289dca09-c957-304e-e063-6394a90a5ca7
Description

100 TABLET in 1 BOTTLE (68071-3739-1)

Marketing

Marketing Status
Marketed Since 2024-12-06
Brand metformin hydrochloride
Generic metformin hydrochloride
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": "289dca09-c957-304e-e063-6394a90a5ca7", "openfda": {"upc": ["0368071373912"], "unii": ["786Z46389E"], "rxcui": ["861007"], "spl_set_id": ["289dc8ec-42c8-1d09-e063-6394a90a97f0"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68071-3739-1)", "package_ndc": "68071-3739-1", "marketing_start_date": "20241206"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "68071-3739_289dca09-c957-304e-e063-6394a90a5ca7", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68071-3739", "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": "500 mg/1"}], "application_number": "ANDA213320", "marketing_category": "ANDA", "marketing_start_date": "20230119", "listing_expiration_date": "20261231"}