Package 68682-018-90

Brand: metformin hydrochloride

Generic: metformin hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68682-018-90
Digits Only 6868201890
Product NDC 68682-018
Product ID 68682-018_26e1cf7e-cc48-cc39-e063-6394a90a62cc
Description

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-018-90)

Marketing

Marketing Status
Marketed Since 2008-06-17
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": "26e1cf7e-cc48-cc39-e063-6394a90a62cc", "openfda": {"unii": ["786Z46389E"], "rxcui": ["1807888", "1807915"], "spl_set_id": ["74d32a8a-c4c2-4dbb-b376-eea3f8fa64d7"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68682-018-90)", "package_ndc": "68682-018-90", "marketing_start_date": "20080617"}], "brand_name": "Metformin hydrochloride", "product_id": "68682-018_26e1cf7e-cc48-cc39-e063-6394a90a62cc", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "68682-018", "generic_name": "metformin hydrochloride", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin hydrochloride", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "NDA021748", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20080617", "listing_expiration_date": "20261231"}