Prednisolone Tebutate

   
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Prednisolone Tebutate


Drug - Prednisolone Tebutate
The trade name of the product as shown on the labeling.

Dosage - INJECTABLE; INJECTION
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Prednisolone Tebutate
Multiple ingredients are in alphabetical order.

Strength - 20MG/ML
The potency of the active ingredient(s), Prednisolone Tebutate. May repeat for multiple part products.

Applicant - STERIS
The firm name holding legal responsibility for Prednisolone Tebutate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 083362
The FDA assigned number to Prednisolone Tebutate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Prednisolone Tebutate. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code -
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Feb 17, 1984
The date Prednisolone Tebutate 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 Prednisolone Tebutate. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - DISCN
The group or category of approved drugs Prednisolone Tebutate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Steris Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Prednisolone Tebutate.

Prednisolone Tebutate