Vancocin Hcl

   
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Vancocin Hcl


Drug - Vancocin Hcl
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) - Vancomycin Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - EQ 500MG BASE/VIAL
The potency of the active ingredient(s), Vancomycin Hydrochloride. May repeat for multiple part products.

Applicant - VIROPHARMA
The firm name holding legal responsibility for Vancocin Hcl. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 062716
The FDA assigned number to Vancocin Hcl. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Vancocin Hcl. 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 - Mar 13, 1987
The date Vancocin Hcl 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 Vancocin Hcl. 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 Vancocin Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Viropharma Inc
The full name of the firm holding legal responsibility for the new application of Vancocin Hcl.

Vancocin Hcl