Package 68462-567-30

Brand: amlodipine and olmesartan medoxomil

Generic: amlodipine and olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 68462-567-30
Digits Only 6846256730
Product NDC 68462-567
Description

30 TABLET, FILM COATED in 1 BOTTLE (68462-567-30)

Marketing

Marketing Status
Marketed Since 2017-07-05
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"}