Package 50090-7681-0

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 50090-7681-0
Digits Only 5009076810
Product NDC 50090-7681
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7681-0)

Marketing

Marketing Status
Marketed Since 2025-10-09
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": "14dd93c4-2a8d-41d7-b844-66b048ef7315", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349405"], "spl_set_id": ["3c001b8d-f6c1-4316-b8c0-590b2fa7f2e5"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7681-0)", "package_ndc": "50090-7681-0", "marketing_start_date": "20251009"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "50090-7681_14dd93c4-2a8d-41d7-b844-66b048ef7315", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-7681", "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": "40 mg/1"}], "application_number": "ANDA211049", "marketing_category": "ANDA", "marketing_start_date": "20190305", "listing_expiration_date": "20261231"}