NuCort - 15014-185-02 - (Hydrocortisone Acetate)

Alphabetical Index


Drug Information of NuCort

Product NDC: 15014-185
Proprietary Name: NuCort
Non Proprietary Name: Hydrocortisone Acetate
Active Ingredient(s): 20    mg/g & nbsp;   Hydrocortisone Acetate
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of NuCort

Product NDC: 15014-185
Labeler Name: Gentex Pharma
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20100816

Package Information of NuCort

Package NDC: 15014-185-02
Package Description: 1 BOTTLE in 1 CARTON (15014-185-02) > 56.7 g in 1 BOTTLE

NDC Information of NuCort

NDC Code 15014-185-02
Proprietary Name NuCort
Package Description 1 BOTTLE in 1 CARTON (15014-185-02) > 56.7 g in 1 BOTTLE
Product NDC 15014-185
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydrocortisone Acetate
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20100816
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Gentex Pharma
Substance Name HYDROCORTISONE ACETATE
Strength Number 20
Strength Unit mg/g
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of NuCort


General Information