Sulten-10

   
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Sulten-10


Drug - Sulten-10
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 - BAUSCH AND LOMB
The firm name holding legal responsibility for Sulten-10. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 087818
The FDA assigned number to Sulten-10. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Sulten-10. 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 - Feb 3, 1983
The date Sulten-10 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 Sulten-10. 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 Sulten-10 is in. Format is RX, OTC, DISCN.

Applicant Full Name - Bausch And Lomb Inc
The full name of the firm holding legal responsibility for the new application of Sulten-10.

Sulten-10