Package 71335-2569-1

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 71335-2569-1
Digits Only 7133525691
Product NDC 71335-2569
Product ID 71335-2569_0f5b17f1-7d06-48f2-88cd-46e4d36d6f83
Description

90 TABLET, COATED in 1 BOTTLE (71335-2569-1)

Marketing

Marketing Status
Discontinued 2026-06-30
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": "0f5b17f1-7d06-48f2-88cd-46e4d36d6f83", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349373"], "spl_set_id": ["ecbb9e05-d590-423f-b530-141f617d5a93"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-2569-1)", "package_ndc": "71335-2569-1", "marketing_end_date": "20260630", "marketing_start_date": "20250205"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "71335-2569_0f5b17f1-7d06-48f2-88cd-46e4d36d6f83", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-2569", "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": "5 mg/1"}], "application_number": "ANDA208659", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20240330"}