Rocaltrol - 0179-0069-70 - (calcitriol)

Alphabetical Index


Drug Information of Rocaltrol

Product NDC: 0179-0069
Proprietary Name: Rocaltrol
Non Proprietary Name: calcitriol
Active Ingredient(s): .25    ug/1 & nbsp;   calcitriol
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, GELATIN COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Rocaltrol

Product NDC: 0179-0069
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018044
Marketing Category: NDA
Start Marketing Date: 20100809

Package Information of Rocaltrol

Package NDC: 0179-0069-70
Package Description: 30 CAPSULE, GELATIN COATED in 1 BOX, UNIT-DOSE (0179-0069-70)

NDC Information of Rocaltrol

NDC Code 0179-0069-70
Proprietary Name Rocaltrol
Package Description 30 CAPSULE, GELATIN COATED in 1 BOX, UNIT-DOSE (0179-0069-70)
Product NDC 0179-0069
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name calcitriol
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20100809
Marketing Category Name NDA
Labeler Name KAISER FOUNDATION HOSPITALS
Substance Name CALCITRIOL
Strength Number .25
Strength Unit ug/1
Pharmaceutical Classes Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC]

Complete Information of Rocaltrol


General Information