Ddavp (needs No Refrigeration)

   
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Ddavp (needs No Refrigeration)


Drug - Ddavp (needs No Refrigeration)
The trade name of the product as shown on the labeling.

Dosage - SPRAY, METERED; NASAL
The product dosage form and route separated by a semi-colon.

Active Ingredient(s) - Desmopressin Acetate
Multiple ingredients are in alphabetical order.

Strength - 0.01MG/SPRAY
The potency of the active ingredient(s), Desmopressin Acetate. May repeat for multiple part products.

Applicant - AVENTIS
The firm name holding legal responsibility for Ddavp (needs No Refrigeration). The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 017922
The FDA assigned number to Ddavp (needs No Refrigeration). Format is nnnnnn.

Product Number - 003
The FDA assigned number to identify Ddavp (needs No Refrigeration). 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 7, 1996
The date Ddavp (needs No Refrigeration) 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 Ddavp (needs No Refrigeration). 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 Ddavp (needs No Refrigeration) is in. Format is RX, OTC, DISCN.

Applicant Full Name - Aventis Pharmaceutical Products Inc
The full name of the firm holding legal responsibility for the new application of Ddavp (needs No Refrigeration).

Ddavp (needs No Refrigeration)