Package 50090-7810-0

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 50090-7810-0
Digits Only 5009078100
Product NDC 50090-7810
Product ID 50090-7810_f6440665-2b7c-48c3-9cdc-f8382a8ebbbb
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7810-0)

Marketing

Marketing Status
Marketed Since 2025-12-05
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": "f6440665-2b7c-48c3-9cdc-f8382a8ebbbb", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349405"], "spl_set_id": ["8acdc142-aa38-4fcb-bd15-fbba9635a4c6"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7810-0)", "package_ndc": "50090-7810-0", "marketing_start_date": "20251205"}], "brand_name": "Olmesartan Medoxomil", "product_id": "50090-7810_f6440665-2b7c-48c3-9cdc-f8382a8ebbbb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-7810", "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": "ANDA203281", "marketing_category": "ANDA", "marketing_start_date": "20170525", "listing_expiration_date": "20261231"}