Package 68071-3526-1
Brand: metformin hydrochloride
Generic: metformin hydrochloridePackage 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
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"}