Package 18124-011-25

Brand: cleviprex

Generic: clevidipine
NDC Package

Package Facts

Identity

Package NDC 18124-011-25
Digits Only 1812401125
Product NDC 18124-011
Description

4 CARTON in 1 CARTON (18124-011-25) / 1 VIAL, SINGLE-USE in 1 CARTON / 250 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2008-09-15
Brand cleviprex
Generic clevidipine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0ef540ec-3e55-44d0-b8b9-e70407a54748", "openfda": {"nui": ["N0000000069", "N0000175421", "M0006414"], "unii": ["19O2GP3B7Q"], "rxcui": ["1790239", "1790242", "1790245", "1790246", "1790247", "1790248"], "spl_set_id": ["a6826aa3-fabb-4ff1-a7a3-cd4c34e3a330"], "pharm_class_cs": ["Dihydropyridines [CS]"], "pharm_class_epc": ["Dihydropyridine Calcium Channel Blocker [EPC]"], "pharm_class_moa": ["Calcium Channel Antagonists [MoA]"], "manufacturer_name": ["Fresenius Kabi Austria GmbH"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 CARTON (18124-011-00)  / 1 VIAL, SINGLE-USE in 1 CARTON / 100 mL in 1 VIAL, SINGLE-USE", "package_ndc": "18124-011-00", "marketing_start_date": "20080915"}, {"sample": false, "description": "4 CARTON in 1 CARTON (18124-011-25)  / 1 VIAL, SINGLE-USE in 1 CARTON / 250 mL in 1 VIAL, SINGLE-USE", "package_ndc": "18124-011-25", "marketing_start_date": "20080915"}, {"sample": false, "description": "10 CARTON in 1 CARTON (18124-011-50)  / 1 VIAL, SINGLE-USE in 1 CARTON / 50 mL in 1 VIAL, SINGLE-USE", "package_ndc": "18124-011-50", "marketing_start_date": "20080915"}], "brand_name": "Cleviprex", "product_id": "18124-011_0ef540ec-3e55-44d0-b8b9-e70407a54748", "dosage_form": "EMULSION", "pharm_class": ["Calcium Channel Antagonists [MoA]", "Dihydropyridine Calcium Channel Blocker [EPC]", "Dihydropyridines [CS]"], "product_ndc": "18124-011", "generic_name": "clevidipine", "labeler_name": "Fresenius Kabi Austria GmbH", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cleviprex", "active_ingredients": [{"name": "CLEVIDIPINE", "strength": ".5 mg/mL"}], "application_number": "NDA022156", "marketing_category": "NDA", "marketing_start_date": "20080915", "listing_expiration_date": "20261231"}