Chloromyxin

   
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Chloromyxin


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

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

Active Ingredient(s) - Chloramphenicol; Polymyxin B Sulfate
Multiple ingredients are in alphabetical order.

Strength - 1%;10,000 UNITS/GM
The potency of the active ingredient(s), Chloramphenicol; Polymyxin B Sulfate. May repeat for multiple part products.

Applicant - PARKE DAVIS
The firm name holding legal responsibility for Chloromyxin. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 050203
The FDA assigned number to Chloromyxin. Format is nnnnnn.

Product Number - 002
The FDA assigned number to identify Chloromyxin. 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 Chloromyxin 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 Chloromyxin. 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 Chloromyxin is in. Format is RX, OTC, DISCN.

Applicant Full Name - Parke Davis Pharmaceutical Research Div Warner Lambert Co
The full name of the firm holding legal responsibility for the new application of Chloromyxin.

Chloromyxin