Package 33342-192-10
Brand: amlodipine and olmesartan medoxomil
Generic: amlodipine and olmesartan medoxomilPackage Facts
Identity
Package NDC
33342-192-10
Digits Only
3334219210
Product NDC
33342-192
Description
90 TABLET, FILM COATED in 1 BOTTLE (33342-192-10)
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": "bd687a21-be18-439a-8e65-103a15b4a8f8", "openfda": {"upc": ["0333342192073", "0333342191076", "0333342192103", "0333342190079", "0333342193100", "0333342191106", "0333342193070", "0333342190109"], "unii": ["864V2Q084H", "6M97XTV3HD"], "rxcui": ["730861", "730866", "730869", "730872"], "spl_set_id": ["c86a3c45-c906-46c9-9f7b-6c3d89bbe48f"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (33342-192-07)", "package_ndc": "33342-192-07", "marketing_start_date": "20161027"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-192-10)", "package_ndc": "33342-192-10", "marketing_start_date": "20161027"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-192-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "33342-192-12", "marketing_start_date": "20161027"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (33342-192-44)", "package_ndc": "33342-192-44", "marketing_start_date": "20161027"}], "brand_name": "AMLODIPINE and OLMESARTAN medoxomil", "product_id": "33342-192_bd687a21-be18-439a-8e65-103a15b4a8f8", "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": "33342-192", "generic_name": "AMLODIPINE and OLMESARTAN medoxomil", "labeler_name": "Macleods Pharmaceuticals 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": "ANDA206884", "marketing_category": "ANDA", "marketing_start_date": "20161027", "listing_expiration_date": "20271231"}