Package 68180-336-07

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68180-336-07
Digits Only 6818033607
Product NDC 68180-336
Description

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-336-07)

Marketing

Marketing Status
Marketed Since 2011-09-30
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": "8d44b37a-b1be-4b0f-808e-70c088f55331", "openfda": {"upc": ["0368180337072"], "unii": ["786Z46389E"], "rxcui": ["1807894", "1807917"], "spl_set_id": ["2a84c550-aed8-4058-961f-351a5e4cf7a1"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-336-07)", "package_ndc": "68180-336-07", "marketing_start_date": "20110930"}], "brand_name": "Metformin Hydrochloride", "product_id": "68180-336_8d44b37a-b1be-4b0f-808e-70c088f55331", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68180-336", "generic_name": "Metformin Hydrochloride", "labeler_name": "Lupin Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin Hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "500 mg/1"}], "application_number": "ANDA090692", "marketing_category": "ANDA", "marketing_start_date": "20110930", "listing_expiration_date": "20261231"}