Alacort - 0316-0126-03 - (Hydrocortisone)

Alphabetical Index


Drug Information of Alacort

Product NDC: 0316-0126
Proprietary Name: Alacort
Non Proprietary Name: Hydrocortisone
Active Ingredient(s): 10    mg/g & nbsp;   Hydrocortisone
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Alacort

Product NDC: 0316-0126
Labeler Name: Crown Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA080706
Marketing Category: ANDA
Start Marketing Date: 19730309

Package Information of Alacort

Package NDC: 0316-0126-03
Package Description: 85.2 g in 1 TUBE (0316-0126-03)

NDC Information of Alacort

NDC Code 0316-0126-03
Proprietary Name Alacort
Package Description 85.2 g in 1 TUBE (0316-0126-03)
Product NDC 0316-0126
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19730309
Marketing Category Name ANDA
Labeler Name Crown Laboratories
Substance Name HYDROCORTISONE
Strength Number 10
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Alacort


General Information