Fluphenazine Hcl

   
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Fluphenazine Hcl


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

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

Active Ingredient(s) - Fluphenazine Hydrochloride
Multiple ingredients are in alphabetical order.

Strength - 10MG
The potency of the active ingredient(s), Fluphenazine Hydrochloride. May repeat for multiple part products.

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

New Drug Application (NDA) Number - 089804
The FDA assigned number to Fluphenazine Hcl. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Fluphenazine Hcl. Each strength is a separate product. May repeat for multiple part products. Format is nnn.

Therapeutic Equivalence (TE) Code - AB
The TE Code indicates the therapeutic equivalence rating of generic to innovator Rx products.

Approval Date - Aug 12, 1988
The date Fluphenazine 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 Fluphenazine Hcl. The RLD identifies the product Abbreviated New Drug Applications (ANDA) use as a reference. Format is Yes or No.

Type - RX
The group or category of approved drugs Fluphenazine Hcl is in. Format is RX, OTC, DISCN.

Applicant Full Name - Mylan Pharmaceuticals Inc
The full name of the firm holding legal responsibility for the new application of Fluphenazine Hcl.

Fluphenazine Hcl