Package 71335-0775-1

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 71335-0775-1
Digits Only 7133507751
Product NDC 71335-0775
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-0775-1)

Marketing

Marketing Status
Marketed Since 2018-04-13
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": "a8d88d67-a666-4e95-b00a-b81c24e52a52", "openfda": {"unii": ["6M97XTV3HD"], "rxcui": ["349401"], "spl_set_id": ["a4ceea38-8fff-4317-be04-8dc22222ec70"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0775-1)", "package_ndc": "71335-0775-1", "marketing_start_date": "20180413"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0775-2)", "package_ndc": "71335-0775-2", "marketing_start_date": "20180808"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0775-3)", "package_ndc": "71335-0775-3", "marketing_start_date": "20200706"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-0775-4)", "package_ndc": "71335-0775-4", "marketing_start_date": "20211227"}], "brand_name": "olmesartan medoxomil", "product_id": "71335-0775_a8d88d67-a666-4e95-b00a-b81c24e52a52", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "71335-0775", "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": "ANDA207662", "marketing_category": "ANDA", "marketing_start_date": "20170427", "listing_expiration_date": "20261231"}