Package 68180-338-01

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68180-338-01
Digits Only 6818033801
Product NDC 68180-338
Product ID 68180-338_2da9ae97-97e8-43fe-b92a-00f3f7c25673
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-338-01)

Marketing

Marketing Status
Marketed Since 2016-02-01
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": "2da9ae97-97e8-43fe-b92a-00f3f7c25673", "openfda": {"unii": ["786Z46389E"], "rxcui": ["1807888", "1807915"], "spl_set_id": ["1200ea71-8a9e-4e49-bb77-7d9fe0d84ae7"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68180-338-01)", "package_ndc": "68180-338-01", "marketing_start_date": "20160201"}], "brand_name": "METFORMIN HYDROCHLORIDE", "product_id": "68180-338_2da9ae97-97e8-43fe-b92a-00f3f7c25673", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68180-338", "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": "ANDA091664", "marketing_category": "ANDA", "marketing_start_date": "20160201", "listing_expiration_date": "20261231"}