Package 71335-2399-3

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 71335-2399-3
Digits Only 7133523993
Product NDC 71335-2399
Description

90 TABLET in 1 BOTTLE (71335-2399-3)

Marketing

Marketing Status
Marketed Since 2024-06-13
Brand olmesartan medoxomil
Generic olmesartan medoxomil
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a638f24b-38b1-4e16-bf18-54d9b99a28d0", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["879630ff-662a-40bd-b74f-a864661dea95"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2399-1)", "package_ndc": "71335-2399-1", "marketing_start_date": "20240613"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2399-2)", "package_ndc": "71335-2399-2", "marketing_start_date": "20240613"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2399-3)", "package_ndc": "71335-2399-3", "marketing_start_date": "20240613"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-2399-4)", "package_ndc": "71335-2399-4", "marketing_start_date": "20240613"}], "brand_name": "OLMESARTAN MEDOXOMIL", "product_id": "71335-2399_a638f24b-38b1-4e16-bf18-54d9b99a28d0", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-2399", "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": "20 mg/1"}], "application_number": "ANDA206720", "marketing_category": "ANDA", "marketing_start_date": "20220304", "listing_expiration_date": "20261231"}