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UticortDrug - Uticort The trade name of the product as shown on the labeling.
Dosage -
LOTION; TOPICAL
Active Ingredient(s) -
Betamethasone Benzoate
Strength -
0.025%
Applicant -
PARKE DAVIS
New Drug Application (NDA) Number -
017528
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Approved Prior to Jan 1, 1982
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Parke Davis Pharmaceutical Research Div Warner Lambert Co
Uticort
Uticort 0.025% Lotion; Topical
Survanta 25mg/ml Suspension; Intratracheal Solatene 30mg Capsule; Oral Cystadane 1gm/scoopful For Solution; Oral Celestone 0.2% Cream; Topical Celestone 0.6mg/5ml Syrup; Oral Celestone 0.6mg Tablet; Oral Celestone Soluspan 3mg/ml;eq 3mg Base/ml Injectable; Injection Uticort 0.025% Cream; Topical Uticort 0.025% Gel; Topical NewDrugInformation |