Package 72189-548-90
Brand: olmesartan medoxomil
Generic: olmesartan medoxomilPackage Facts
Identity
Package NDC
72189-548-90
Digits Only
7218954890
Product NDC
72189-548
Description
90 TABLET, FILM COATED in 1 BOTTLE (72189-548-90)
Marketing
Marketing Status
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": "16752f60-655b-f727-e063-6394a90a96b6", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["16752f60-655a-f727-e063-6394a90a96b6"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-548-90)", "package_ndc": "72189-548-90", "marketing_start_date": "20240419"}], "brand_name": "Olmesartan Medoxomil", "product_id": "72189-548_16752f60-655b-f727-e063-6394a90a96b6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-548", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA204798", "marketing_category": "ANDA", "marketing_start_date": "20240419", "listing_expiration_date": "20261231"}