Package 42571-236-10

Brand: amlodipine and olmesartan medoxomil

Generic: amlodipine and olmesartan medoxomil
NDC Package

Package Facts

Identity

Package NDC 42571-236-10
Digits Only 4257123610
Product NDC 42571-236
Description

1000 TABLET in 1 BOTTLE (42571-236-10)

Marketing

Marketing Status
Marketed Since 2018-01-01
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": "2b531912-67b1-6172-e063-6394a90a178f", "openfda": {"upc": ["0342571238308", "0342571237301", "0342571235307", "0342571236304"], "unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730861", "730866", "730869", "730872"], "spl_set_id": ["7fcf6a87-7b3e-4cef-8c47-c8a008cfea82"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (42571-236-05)", "package_ndc": "42571-236-05", "marketing_start_date": "20180101"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (42571-236-10)", "package_ndc": "42571-236-10", "marketing_start_date": "20180101"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (42571-236-30)", "package_ndc": "42571-236-30", "marketing_start_date": "20180101"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (42571-236-90)", "package_ndc": "42571-236-90", "marketing_start_date": "20180101"}], "brand_name": "AMLODIPINE AND OLMESARTAN MEDOXOMIL", "product_id": "42571-236_2b531912-67b1-6172-e063-6394a90a178f", "dosage_form": "TABLET", "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": "42571-236", "generic_name": "Amlodipine and Olmesartan Medoxomil", "labeler_name": "Micro Labs Limited", "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": "ANDA207435", "marketing_category": "ANDA", "marketing_start_date": "20180101", "listing_expiration_date": "20261231"}