Prostaphlin

   
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Prostaphlin


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

Dosage - FOR SOLUTION; ORAL
The product dosage form and route separated by a semi-colon.

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

Strength - EQ 250MG BASE/5ML
The potency of the active ingredient(s), Oxacillin Sodium. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 050194
The FDA assigned number to Prostaphlin. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Prostaphlin. 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 Prostaphlin 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 Prostaphlin. 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 Prostaphlin is in. Format is RX, OTC, DISCN.

Applicant Full Name - Apothecon Inc Div Bristol Myers Squibb
The full name of the firm holding legal responsibility for the new application of Prostaphlin.

Prostaphlin