Package 71335-2600-1

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 71335-2600-1
Digits Only 7133526001
Product NDC 71335-2600
Product ID 71335-2600_c9a7aa4e-1d94-4f7e-a368-316d794083c4
Description

90 TABLET, COATED in 1 BOTTLE (71335-2600-1)

Marketing

Marketing Status
Marketed Since 2025-06-05
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": "c9a7aa4e-1d94-4f7e-a368-316d794083c4", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349373"], "spl_set_id": ["eff499eb-a0e4-4240-870c-83bb53434cc2"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-2600-1)", "package_ndc": "71335-2600-1", "marketing_start_date": "20250605"}], "brand_name": "Olmesartan Medoxomil", "product_id": "71335-2600_c9a7aa4e-1d94-4f7e-a368-316d794083c4", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-2600", "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": "ANDA206763", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}