Package 62756-142-01

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62756-142-01
Digits Only 6275614201
Product NDC 62756-142
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-01)

Marketing

Marketing Status
Marketed Since 2006-02-09
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": "69a60382-bf12-4627-baaf-2e0ac332b443", "openfda": {"upc": ["0362756142015", "0362756143012"], "unii": ["786Z46389E"], "spl_set_id": ["41a8bb80-7b0b-476c-8134-5d161c3239c8"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-01)", "package_ndc": "62756-142-01", "marketing_start_date": "20060209"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (62756-142-02)", "package_ndc": "62756-142-02", "marketing_start_date": "20060209"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "62756-142_69a60382-bf12-4627-baaf-2e0ac332b443", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "62756-142", "generic_name": "METFORMIN HYDROCHLORIDE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METFORMIN HYDROCHLORIDE", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA077336", "marketing_category": "ANDA", "marketing_start_date": "20060209", "listing_expiration_date": "20261231"}