Package 50228-365-90
Brand: amlodipine and olmesartan medoxomil
Generic: amlodipine and olmesartan medoxomilPackage Facts
Identity
Package NDC
50228-365-90
Digits Only
5022836590
Product NDC
50228-365
Description
90 TABLET, FILM COATED in 1 BOTTLE (50228-365-90)
Marketing
Marketing Status
Brand
amlodipine and olmesartan medoxomil
Generic
amlodipine and olmesartan medoxomil
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1666c9c9-9d30-4155-e063-6394a90afde9", "openfda": {"upc": ["0350228367103", "0350228367301", "0350228366106", "0350228365109", "0350228368100", "0350228366908", "0350228365307", "0350228366304", "0350228368902", "0350228365901", "0350228368308", "0350228367905"], "unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730861", "730866", "730869", "730872"], "spl_set_id": ["c531fceb-09aa-492b-a5a3-2b004e9eadda"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (50228-365-10)", "package_ndc": "50228-365-10", "marketing_start_date": "20181203"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50228-365-30)", "package_ndc": "50228-365-30", "marketing_start_date": "20181203"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50228-365-90)", "package_ndc": "50228-365-90", "marketing_start_date": "20181203"}], "brand_name": "Amlodipine and Olmesartan Medoxomil", "product_id": "50228-365_1666c9c9-9d30-4155-e063-6394a90afde9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Calcium Channel Antagonists [MoA]", "Calcium Channel Blocker [EPC]", "Cytochrome P450 3A Inhibitors [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "50228-365", "generic_name": "Amlodipine and Olmesartan Medoxomil", "labeler_name": "ScieGen Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Olmesartan Medoxomil", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA209010", "marketing_category": "ANDA", "marketing_start_date": "20181203", "listing_expiration_date": "20261231"}