Package 42708-018-30

Brand: metformin hcl

Generic: metformin hcl
NDC Package Sample

Package Facts

Identity

Package NDC 42708-018-30
Digits Only 4270801830
Product NDC 42708-018
Description

30 TABLET in 1 BOTTLE (42708-018-30)

Marketing

Marketing Status
Marketed Since 2018-07-30
Brand metformin hcl
Generic metformin hcl
Sample Package Yes

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "45b422ff-1892-ceaa-e063-6394a90a00c9", "openfda": {"unii": ["786Z46389E"], "rxcui": ["861004", "861007"], "spl_set_id": ["06ade2e1-5981-4e3d-b7e9-7ff083eb4551"], "manufacturer_name": ["QPharma, Inc."]}, "finished": true, "packaging": [{"sample": true, "description": "30 TABLET in 1 BOTTLE (42708-018-30)", "package_ndc": "42708-018-30", "marketing_start_date": "20180730"}], "brand_name": "Metformin HCl", "product_id": "42708-018_45b422ff-1892-ceaa-e063-6394a90a00c9", "dosage_form": "TABLET", "pharm_class": ["Biguanide [EPC]", "Biguanides [CS]"], "product_ndc": "42708-018", "generic_name": "Metformin HCl", "labeler_name": "QPharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metformin HCl", "active_ingredients": [{"name": "METFORMIN HYDROCHLORIDE", "strength": "1000 mg/1"}], "application_number": "ANDA090564", "marketing_category": "ANDA", "marketing_start_date": "20170206", "listing_expiration_date": "20261231"}