Meti-derm

   
Google
 
Web NewDrugInformation.com

Meti-derm


Drug - Meti-derm
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) - Prednisolone
Multiple ingredients are in alphabetical order.

Strength - 0.5%
The potency of the active ingredient(s), Prednisolone. May repeat for multiple part products.

Applicant - SCHERING
The firm name holding legal responsibility for Meti-derm. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 010209
The FDA assigned number to Meti-derm. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Meti-derm. 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 - Approved Prior to Jan 1, 1982
The date Meti-derm 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 Meti-derm. 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 Meti-derm is in. Format is RX, OTC, DISCN.

Applicant Full Name - Schering Corp Sub Schering Plough Corp
The full name of the firm holding legal responsibility for the new application of Meti-derm.

Meti-derm