|
WestcortDrug - Westcort The trade name of the product as shown on the labeling.
Dosage -
OINTMENT; TOPICAL
Active Ingredient(s) -
Hydrocortisone Valerate
Strength -
0.2%
Applicant -
WESTWOOD SQUIBB
New Drug Application (NDA) Number -
018726
Product Number -
001
Therapeutic Equivalence (TE) Code -
AB
Approval Date -
Aug 8, 1983
Reference Listed Drug (RLD) -
Yes
Type -
RX
Applicant Full Name -
Westwood Squibb Pharmaceuticals Inc
Westcort
Solu-cortef Eq 500mg Base/vial Injectable; Injection
Hydrocortisone Valerate 0.2% Cream; Topical Hydrocortisone Valerate 0.2% Cream; Topical Hydrocortisone Valerate 0.2% Cream; Topical Westcort 0.2% Cream; Topical Hydrocortisone Valerate 0.2% Ointment; Topical Hydrocortisone Valerate 0.2% Ointment; Topical Westcort 0.2% Ointment; Topical Solu-cortef Eq 1gm Base/vial Injectable; Injection Solu-cortef Eq 250mg Base/vial Injectable; Injection NewDrugInformation |