Package 72189-373-90

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 72189-373-90
Digits Only 7218937390
Product NDC 72189-373
Product ID 72189-373_2c4cb2f6-84b2-31c2-e063-6394a90a5568
Description

90 TABLET, FILM COATED in 1 BOTTLE (72189-373-90)

Marketing

Marketing Status
Marketed Since 2022-08-15
Brand olmesartan medoxomil
Generic olmesartan medoxomil
Sample Package No

Linked Drug Pages (1)

Olmesartan Medoxomil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4cb2f6-84b2-31c2-e063-6394a90a5568", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349373"], "spl_set_id": ["e64c3b3b-d5e7-6d46-e053-2a95a90a1b64"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-373-90)", "package_ndc": "72189-373-90", "marketing_start_date": "20220815"}], "brand_name": "Olmesartan Medoxomil", "product_id": "72189-373_2c4cb2f6-84b2-31c2-e063-6394a90a5568", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "72189-373", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "5 mg/1"}], "application_number": "ANDA207662", "marketing_category": "ANDA", "marketing_start_date": "20220815", "listing_expiration_date": "20261231"}