Pred Mild

   
Google
 
Web NewDrugInformation.com

Pred Mild


Drug - Pred Mild
The trade name of the product as shown on the labeling.

Dosage - SUSPENSION/DROPS; OPHTHALMIC
The product dosage form and route separated by a semi-colon.

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

Strength - 0.12%
The potency of the active ingredient(s), Prednisolone Acetate. May repeat for multiple part products.

Applicant - ALLERGAN
The firm name holding legal responsibility for Pred Mild. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 017100
The FDA assigned number to Pred Mild. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Pred Mild. 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 Pred Mild 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) - Yes
The pioneer or innovator of Pred Mild. 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 Pred Mild is in. Format is RX, OTC, DISCN.

Applicant Full Name - Allergan Pharmaceutical
The full name of the firm holding legal responsibility for the new application of Pred Mild.

Pred Mild