CALCITRIOL - 63304-241-59 - (CALCITRIOL)

Alphabetical Index


Drug Information of CALCITRIOL

Product NDC: 63304-241
Proprietary Name: CALCITRIOL
Non Proprietary Name: CALCITRIOL
Active Ingredient(s): 1    ug/mL & nbsp;   CALCITRIOL
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of CALCITRIOL

Product NDC: 63304-241
Labeler Name: Ranbaxy Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021068
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20090826

Package Information of CALCITRIOL

Package NDC: 63304-241-59
Package Description: 15 mL in 1 BOTTLE (63304-241-59)

NDC Information of CALCITRIOL

NDC Code 63304-241-59
Proprietary Name CALCITRIOL
Package Description 15 mL in 1 BOTTLE (63304-241-59)
Product NDC 63304-241
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CALCITRIOL
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20090826
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Ranbaxy Pharmaceuticals Inc.
Substance Name CALCITRIOL
Strength Number 1
Strength Unit ug/mL
Pharmaceutical Classes Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC]

Complete Information of CALCITRIOL


General Information