Package 65862-742-90

Brand: olmesartan medoxomil

Generic: olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 65862-742-90
Digits Only 6586274290
Product NDC 65862-742
Description

90 TABLET, FILM COATED in 1 BOTTLE (65862-742-90)

Marketing

Marketing Status
Marketed Since 2017-04-24
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": "6135c8a8-0232-4aa1-be56-8c29a444d96f", "openfda": {"upc": ["0365862742308", "0365862743305", "0365862741301"], "unii": ["6M97XTV3HD"], "rxcui": ["349373", "349401", "349405"], "spl_set_id": ["8c94d403-809b-43b9-834f-3ecd330d2dd9"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-742-01)", "package_ndc": "65862-742-01", "marketing_start_date": "20170424"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65862-742-05)", "package_ndc": "65862-742-05", "marketing_start_date": "20170424"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-742-30)", "package_ndc": "65862-742-30", "marketing_start_date": "20170424"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-742-78)  / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-742-10)", "package_ndc": "65862-742-78", "marketing_start_date": "20170424"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-742-90)", "package_ndc": "65862-742-90", "marketing_start_date": "20170424"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-742-99)", "package_ndc": "65862-742-99", "marketing_start_date": "20170424"}], "brand_name": "Olmesartan Medoxomil", "product_id": "65862-742_6135c8a8-0232-4aa1-be56-8c29a444d96f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "65862-742", "generic_name": "Olmesartan Medoxomil", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil", "active_ingredients": [{"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA204798", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}