Westcort - 10631-105-45 - (Hydrocortisone valerate)

Alphabetical Index


Drug Information of Westcort

Product NDC: 10631-105
Proprietary Name: Westcort
Non Proprietary Name: Hydrocortisone valerate
Active Ingredient(s): 2    mg/g & nbsp;   Hydrocortisone valerate
Administration Route(s): TOPICAL
Dosage Form(s): OINTMENT
Coding System: National Drug Codes(NDC)

Labeler Information of Westcort

Product NDC: 10631-105
Labeler Name: Ranbaxy Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018726
Marketing Category: NDA
Start Marketing Date: 20081006

Package Information of Westcort

Package NDC: 10631-105-45
Package Description: 45 g in 1 TUBE (10631-105-45)

NDC Information of Westcort

NDC Code 10631-105-45
Proprietary Name Westcort
Package Description 45 g in 1 TUBE (10631-105-45)
Product NDC 10631-105
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone valerate
Dosage Form Name OINTMENT
Route Name TOPICAL
Start Marketing Date 20081006
Marketing Category Name NDA
Labeler Name Ranbaxy Laboratories Inc.
Substance Name HYDROCORTISONE VALERATE
Strength Number 2
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Westcort


General Information