Zemplar - 0074-4317-30 - (Paricalcitol)

Alphabetical Index


Drug Information of Zemplar

Product NDC: 0074-4317
Proprietary Name: Zemplar
Non Proprietary Name: Paricalcitol
Active Ingredient(s): 1    ug/1 & nbsp;   Paricalcitol
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Zemplar

Product NDC: 0074-4317
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021606
Marketing Category: NDA
Start Marketing Date: 20100614

Package Information of Zemplar

Package NDC: 0074-4317-30
Package Description: 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (0074-4317-30)

NDC Information of Zemplar

NDC Code 0074-4317-30
Proprietary Name Zemplar
Package Description 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (0074-4317-30)
Product NDC 0074-4317
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Paricalcitol
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20100614
Marketing Category Name NDA
Labeler Name AbbVie Inc.
Substance Name PARICALCITOL
Strength Number 1
Strength Unit ug/1
Pharmaceutical Classes Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC]

Complete Information of Zemplar


General Information