Plaquenil

   
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Plaquenil


Drug - Plaquenil
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) - Hydroxychloroquine Sulfate
Multiple ingredients are in alphabetical order.

Strength - 200MG
The potency of the active ingredient(s), Hydroxychloroquine Sulfate. May repeat for multiple part products.

Applicant - SANOFI SYNTHELABO
The firm name holding legal responsibility for Plaquenil. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 009768
The FDA assigned number to Plaquenil. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Plaquenil. 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 - Approved Prior to Jan 1, 1982
The date Plaquenil 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) - Yes
The pioneer or innovator of Plaquenil. 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 Plaquenil is in. Format is RX, OTC, DISCN.

Applicant Full Name - Sanofi Synthelabo Inc
The full name of the firm holding legal responsibility for the new application of Plaquenil.

Plaquenil