Diflorasone Diacetate
Drug - Diflorasone Diacetate
The trade name of the product as shown on the labeling.
Dosage -
CREAM; TOPICAL
The product dosage form and route separated by a semi-colon.
Active Ingredient(s) -
Diflorasone Diacetate
Multiple ingredients are in alphabetical order.
Strength -
0.05%
The potency of the active ingredient(s), Diflorasone Diacetate. May repeat for multiple part products.
Applicant -
TARO
The firm name holding legal responsibility for Diflorasone Diacetate. The firm name is condensed to a maximum twenty character unique string.
New Drug Application (NDA) Number -
075508
The FDA assigned number to Diflorasone Diacetate. Format is nnnnnn.
Product Number -
001
The FDA assigned number to identify Diflorasone Diacetate. Each strength is a separate product. May repeat for multiple part products. Format is nnn.
Therapeutic Equivalence (TE) Code -
AB1
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.
Approval Date -
Apr 24, 2000
The date Diflorasone Diacetate was approved as stated in the FDA approval letter to the applicant. The format is Mmm dd, yyyy. Products approved prior to the January 1, 1982 contain the phrase: "Approved prior to Jan 1, 1982".
Reference Listed Drug (RLD) -
No
The pioneer or innovator of Diflorasone Diacetate. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.
Type -
RX
The group or category of approved drugs Diflorasone Diacetate is in. Format is RX, OTC, DISCN.
Applicant Full Name -
Taro Pharmaceuticals Usa Inc
The full name of the firm holding legal responsibility for the new application of Diflorasone Diacetate.
Diflorasone Diacetate
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