Zemplar - 0074-1658-05 - (Paricalcitol)

Alphabetical Index


Drug Information of Zemplar

Product NDC: 0074-1658
Proprietary Name: Zemplar
Non Proprietary Name: Paricalcitol
Active Ingredient(s): 5    ug/mL & nbsp;   Paricalcitol
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Zemplar

Product NDC: 0074-1658
Labeler Name: Abbott Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020819
Marketing Category: NDA
Start Marketing Date: 19980417

Package Information of Zemplar

Package NDC: 0074-1658-05
Package Description: 25 VIAL, MULTI-DOSE in 1 TRAY (0074-1658-05) > 2 mL in 1 VIAL, MULTI-DOSE

NDC Information of Zemplar

NDC Code 0074-1658-05
Proprietary Name Zemplar
Package Description 25 VIAL, MULTI-DOSE in 1 TRAY (0074-1658-05) > 2 mL in 1 VIAL, MULTI-DOSE
Product NDC 0074-1658
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paricalcitol
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 19980417
Marketing Category Name NDA
Labeler Name Abbott Laboratories
Substance Name PARICALCITOL
Strength Number 5
Strength Unit ug/mL
Pharmaceutical Classes Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC]

Complete Information of Zemplar


General Information