Package 63629-8522-1

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 63629-8522-1
Digits Only 6362985221
Product NDC 63629-8522
Product ID 63629-8522_63fab6d4-0622-40d9-ace7-3c125cd5dbe0
Description

90 TABLET, FILM COATED in 1 BOTTLE (63629-8522-1)

Marketing

Marketing Status
Marketed Since 2021-05-19
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": "63fab6d4-0622-40d9-ace7-3c125cd5dbe0", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["fe80fd21-fa8d-474e-ac0a-23f0e1eb7f3b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-8522-1)", "package_ndc": "63629-8522-1", "marketing_start_date": "20210519"}], "brand_name": "olmesartan medoxomil", "product_id": "63629-8522_63fab6d4-0622-40d9-ace7-3c125cd5dbe0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "63629-8522", "generic_name": "olmesartan medoxomil", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA208130", "marketing_category": "ANDA", "marketing_start_date": "20180629", "listing_expiration_date": "20261231"}