Sulfacetamide Sodium


Sulfacetamide Sodium

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

The product dosage form and route separated by a semi-colon.

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

Strength - 30%
The potency of the active ingredient(s), Sulfacetamide Sodium. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 089068
The FDA assigned number to Sulfacetamide Sodium. Format is nnnnnn.

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

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

Approval Date - May 5, 1987
The date Sulfacetamide Sodium 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 Sulfacetamide Sodium. 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 Sulfacetamide Sodium 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 Sulfacetamide Sodium.

Sulfacetamide Sodium