Package 70882-125-30

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70882-125-30
Digits Only 7088212530
Product NDC 70882-125
Product ID 70882-125_61b6dfd4-ea72-40f3-b4cd-0a51e8a810a6
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70882-125-30)

Marketing

Marketing Status
Marketed Since 2011-01-31
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": "61b6dfd4-ea72-40f3-b4cd-0a51e8a810a6", "openfda": {"upc": ["0370882125307"], "unii": ["786Z46389E"], "rxcui": ["861010"], "spl_set_id": ["9c333ae3-a4df-483b-9103-762134add15e"], "manufacturer_name": ["Cambridge Therapeutics Technologies, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70882-125-30)", "package_ndc": "70882-125-30", "marketing_start_date": "20110131"}], "brand_name": "Metformin Hydrochloride", "product_id": "70882-125_61b6dfd4-ea72-40f3-b4cd-0a51e8a810a6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "70882-125", "generic_name": "Metformin Hydrochloride", "labeler_name": "Cambridge Therapeutics Technologies, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "850 mg/1"}], "application_number": "ANDA091184", "marketing_category": "ANDA", "marketing_start_date": "20110131", "listing_expiration_date": "20261231"}