Package 72189-549-90

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 72189-549-90
Digits Only 7218954990
Product NDC 72189-549
Description

90 TABLET, FILM COATED in 1 BOTTLE (72189-549-90)

Marketing

Marketing Status
Marketed Since 2024-04-19
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": "23080f85-3974-7803-e063-6394a90aa11d", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349405"], "spl_set_id": ["16754802-d5a4-0350-e063-6394a90aa967"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-549-30)", "package_ndc": "72189-549-30", "marketing_start_date": "20240419"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-549-90)", "package_ndc": "72189-549-90", "marketing_start_date": "20240419"}], "brand_name": "Olmesartan Medoxomil", "product_id": "72189-549_23080f85-3974-7803-e063-6394a90aa11d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-549", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA204798", "marketing_category": "ANDA", "marketing_start_date": "20240419", "listing_expiration_date": "20261231"}