Package 50090-6606-0

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 50090-6606-0
Digits Only 5009066060
Product NDC 50090-6606
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-6606-0)

Marketing

Marketing Status
Marketed Since 2023-08-22
Brand olmesartan medoxomil
Generic olmesartan medoxomil
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "63e7c4d9-eb3e-47da-8807-234bd7df2977", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["949e6bad-fcb2-42f2-b9c8-e5620ef5ccd5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-6606-0)", "package_ndc": "50090-6606-0", "marketing_start_date": "20230822"}], "brand_name": "olmesartan medoxomil", "product_id": "50090-6606_63e7c4d9-eb3e-47da-8807-234bd7df2977", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-6606", "generic_name": "olmesartan medoxomil", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA207662", "marketing_category": "ANDA", "marketing_start_date": "20170427", "listing_expiration_date": "20261231"}