Package 68645-300-59

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68645-300-59
Digits Only 6864530059
Product NDC 68645-300
Product ID 68645-300_474350e4-2e45-bec1-e063-6294a90a1154
Description

60 TABLET, FILM COATED in 1 BOTTLE (68645-300-59)

Marketing

Marketing Status
Marketed Since 2012-01-13
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": "474350e4-2e45-bec1-e063-6294a90a1154", "openfda": {"upc": ["0368645300597"], "unii": ["786Z46389E"], "rxcui": ["861004"], "spl_set_id": ["3814cfed-029f-4231-bba3-89b2b4e01392"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68645-300-59)", "package_ndc": "68645-300-59", "marketing_start_date": "20120113"}], "brand_name": "Metformin Hydrochloride", "product_id": "68645-300_474350e4-2e45-bec1-e063-6294a90a1154", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68645-300", "generic_name": "Metformin Hydrochloride", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA077095", "marketing_category": "ANDA", "marketing_start_date": "20120113", "listing_expiration_date": "20261231"}