Package 68462-567-14
Brand: amlodipine and olmesartan medoxomil
Generic: amlodipine and olmesartan medoxomilPackage Facts
Identity
Package NDC
68462-567-14
Digits Only
6846256714
Product NDC
68462-567
Description
10 BLISTER PACK in 1 CARTON (68462-567-14) / 10 TABLET, FILM COATED in 1 BLISTER PACK
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": "6de4a776-9973-4410-ae04-99544813d920", "openfda": {"upc": ["0368462568309", "0368462567302", "0368462569306", "0368462566305"], "unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730861", "730866", "730869", "730872"], "spl_set_id": ["2edf43fb-0755-4ffb-bc38-75a4e2432588"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (68462-567-14) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "68462-567-14", "marketing_start_date": "20170705"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68462-567-30)", "package_ndc": "68462-567-30", "marketing_start_date": "20170705"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68462-567-90)", "package_ndc": "68462-567-90", "marketing_start_date": "20170705"}], "brand_name": "Amlodipine and Olmesartan Medoxomil", "product_id": "68462-567_6de4a776-9973-4410-ae04-99544813d920", "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": "68462-567", "generic_name": "Amlodipine and Olmesartan Medoxomil", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Amlodipine and Olmesartan Medoxomil", "active_ingredients": [{"name": "AMLODIPINE BESYLATE", "strength": "10 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA207807", "marketing_category": "ANDA", "marketing_start_date": "20170705", "listing_expiration_date": "20261231"}