Predamide

   
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Predamide


Drug - Predamide
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; Sulfacetamide Sodium
Multiple ingredients are in alphabetical order.

Strength - 0.5%;10%
The potency of the active ingredient(s), Prednisolone Acetate; Sulfacetamide Sodium. May repeat for multiple part products.

Applicant - AKORN
The firm name holding legal responsibility for Predamide. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 088059
The FDA assigned number to Predamide. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Predamide. 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 - Jul 29, 1983
The date Predamide 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 Predamide. 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 Predamide is in. Format is RX, OTC, DISCN.

Applicant Full Name - Akorn Inc
The full name of the firm holding legal responsibility for the new application of Predamide.

Predamide