Package 71335-2376-1

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 71335-2376-1
Digits Only 7133523761
Product NDC 71335-2376
Product ID 71335-2376_90e7b0d8-5a1e-4ba2-8313-39ba6381ab7c
Description

90 TABLET, FILM COATED in 1 BOTTLE (71335-2376-1)

Marketing

Marketing Status
Marketed Since 2024-05-23
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": "90e7b0d8-5a1e-4ba2-8313-39ba6381ab7c", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349373"], "spl_set_id": ["57dc737b-01e2-4b22-991f-d4710950dcf3"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2376-1)", "package_ndc": "71335-2376-1", "marketing_start_date": "20240523"}], "brand_name": "Olmesartan Medoxomil", "product_id": "71335-2376_90e7b0d8-5a1e-4ba2-8313-39ba6381ab7c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-2376", "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": "ANDA203281", "marketing_category": "ANDA", "marketing_start_date": "20170525", "listing_expiration_date": "20261231"}