Package 71335-2996-1

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 71335-2996-1
Digits Only 7133529961
Product NDC 71335-2996
Product ID 71335-2996_e793346b-0c4d-4377-aff6-a3cd636e1a66
Description

90 TABLET, COATED in 1 BOTTLE (71335-2996-1)

Marketing

Marketing Status
Marketed Since 2026-02-04
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": "e793346b-0c4d-4377-aff6-a3cd636e1a66", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349373"], "spl_set_id": ["1df1ff60-6be5-4018-a28c-0d23e5867eba"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (71335-2996-1)", "package_ndc": "71335-2996-1", "marketing_start_date": "20260204"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "71335-2996_e793346b-0c4d-4377-aff6-a3cd636e1a66", "dosage_form": "TABLET, COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-2996", "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_start_date": "20241007", "listing_expiration_date": "20271231"}