Package 51407-197-30

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 51407-197-30
Digits Only 5140719730
Product NDC 51407-197
Description

30 TABLET, FILM COATED in 1 BOTTLE (51407-197-30)

Marketing

Marketing Status
Marketed Since 2019-02-25
Brand olmesartan medoxomil
Generic olmesartan medoxomil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "44718755-5055-82a4-e063-6294a90a6f7b", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["865c2765-5072-d029-e053-2a91aa0a098e"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51407-197-30)", "package_ndc": "51407-197-30", "marketing_start_date": "20190225"}], "brand_name": "olmesartan medoxomil", "product_id": "51407-197_44718755-5055-82a4-e063-6294a90a6f7b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "51407-197", "generic_name": "olmesartan medoxomil", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "5 mg/1"}], "application_number": "ANDA208130", "marketing_category": "ANDA", "marketing_start_date": "20180629", "listing_expiration_date": "20261231"}