Viocin Sulfate

   
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Viocin Sulfate


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

Dosage - INJECTABLE; INJECTION
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Viomycin Sulfate
Multiple ingredients are in alphabetical order.

Strength - EQ 5GM BASE/VIAL
The potency of the active ingredient(s), Viomycin Sulfate. May repeat for multiple part products.

Applicant - PFIZER
The firm name holding legal responsibility for Viocin Sulfate. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 061086
The FDA assigned number to Viocin Sulfate. Format is nnnnnn.

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

Applicant Full Name - Pfizer Laboratories Div Pfizer Inc
The full name of the firm holding legal responsibility for the new application of Viocin Sulfate.

Viocin Sulfate