Rocaltrol - 30698-143-01 - (calcitriol)

Alphabetical Index


Drug Information of Rocaltrol

Product NDC: 30698-143
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: 30698-143
Labeler Name: Validus Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018044
Marketing Category: NDA
Start Marketing Date: 20090810

Package Information of Rocaltrol

Package NDC: 30698-143-01
Package Description: 100 CAPSULE, GELATIN COATED in 1 BOTTLE (30698-143-01)

NDC Information of Rocaltrol

NDC Code 30698-143-01
Proprietary Name Rocaltrol
Package Description 100 CAPSULE, GELATIN COATED in 1 BOTTLE (30698-143-01)
Product NDC 30698-143
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name calcitriol
Dosage Form Name CAPSULE, GELATIN COATED
Route Name ORAL
Start Marketing Date 20090810
Marketing Category Name NDA
Labeler Name Validus Pharmaceuticals LLC
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