Vincristine Sulfate

   
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Vincristine Sulfate


Drug - Vincristine 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) - Vincristine Sulfate
Multiple ingredients are in alphabetical order.

Strength - 1MG/ML
The potency of the active ingredient(s), Vincristine Sulfate. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 070873
The FDA assigned number to Vincristine Sulfate. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Vincristine 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 - Feb 19, 1987
The date Vincristine 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 Vincristine 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 Vincristine Sulfate is in. Format is RX, OTC, DISCN.

Applicant Full Name - Abic Ltd
The full name of the firm holding legal responsibility for the new application of Vincristine Sulfate.

Vincristine Sulfate