Package 71709-110-07

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71709-110-07
Digits Only 7170911007
Product NDC 71709-110
Product ID 71709-110_63699815-ee85-645d-e053-2a91aa0a7c4f
Description

1000 TABLET, FILM COATED in 1 BOTTLE (71709-110-07)

Marketing

Marketing Status
Marketed Since 2017-11-14
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": "63699815-ee85-645d-e053-2a91aa0a7c4f", "openfda": {"upc": ["0371709110063", "0371709111060"], "unii": ["786Z46389E"], "rxcui": ["861004", "861007", "861010"], "spl_set_id": ["5df6adc9-79fd-66ef-e053-2991aa0a75ce"], "manufacturer_name": ["Metcure Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71709-110-06)", "package_ndc": "71709-110-06", "marketing_start_date": "20171114"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (71709-110-07)", "package_ndc": "71709-110-07", "marketing_start_date": "20171114"}], "brand_name": "Metformin Hydrochloride", "product_id": "71709-110_63699815-ee85-645d-e053-2a91aa0a7c4f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "71709-110", "generic_name": "Metformin Hydrochloride", "labeler_name": "Metcure Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA090564", "marketing_category": "ANDA", "marketing_start_date": "20171114", "listing_expiration_date": "20261231"}