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DermatopDrug - Dermatop The trade name of the product as shown on the labeling.
Dosage -
OINTMENT; TOPICAL
Active Ingredient(s) -
Prednicarbate
Strength -
0.1%
Applicant -
DERMIK LABS
New Drug Application (NDA) Number -
019568
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Sep 23, 1991
Reference Listed Drug (RLD) -
Yes
Type -
RX
Applicant Full Name -
Dermik Laboratories Div Aventis Pharmaceuticals Inc
Dermatop
Prazosin Hcl Eq 5mg Base Capsule; Oral
Prazosin Hcl Eq 1mg Base Capsule; Oral Prazosin Hcl Eq 2mg Base Capsule; Oral Prazosin Hcl Eq 5mg Base Capsule; Oral Minipress Xl 2.5mg Tablet, Extended Release; Oral Minipress Xl 5mg Tablet, Extended Release; Oral Dermatop E Emollient 0.1% Cream; Topical Dermatop 0.1% Ointment; Topical Prazosin Hcl Eq 1mg Base Capsule; Oral Prazosin Hcl Eq 2mg Base Capsule; Oral NewDrugInformation |