Sodium Sulfacetamide

   
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Sodium Sulfacetamide


Drug - Sodium Sulfacetamide
The trade name of the product as shown on the labeling.

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

Active Ingredient(s) - Sulfacetamide Sodium
Multiple ingredients are in alphabetical order.

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

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

New Drug Application (NDA) Number - 083021
The FDA assigned number to Sodium Sulfacetamide. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Sodium Sulfacetamide. 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 Sodium Sulfacetamide 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 Sodium Sulfacetamide. 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 Sodium Sulfacetamide 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 Sodium Sulfacetamide.

Sodium Sulfacetamide