Rauserpin

   
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Rauserpin


Drug - Rauserpin
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) - Rauwolfia Serpentina
Multiple ingredients are in alphabetical order.

Strength - 100MG
The potency of the active ingredient(s), Rauwolfia Serpentina. May repeat for multiple part products.

Applicant - FERNDALE LABS
The firm name holding legal responsibility for Rauserpin. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 009926
The FDA assigned number to Rauserpin. Format is nnnnnn.

Product Number - 004
The FDA assigned number to identify Rauserpin. 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 Rauserpin 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 Rauserpin. 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 Rauserpin is in. Format is RX, OTC, DISCN.

Applicant Full Name - Ferndale Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Rauserpin.

Rauserpin