Desmopressin Acetate Preservative Free

   
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Desmopressin Acetate Preservative Free


Drug - Desmopressin Acetate Preservative Free
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) - Desmopressin Acetate
Multiple ingredients are in alphabetical order.

Strength - 0.004MG/ML
The potency of the active ingredient(s), Desmopressin Acetate. May repeat for multiple part products.

Applicant - BEDFORD
The firm name holding legal responsibility for Desmopressin Acetate Preservative Free. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 074574
The FDA assigned number to Desmopressin Acetate Preservative Free. Format is nnnnnn.

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

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

Approval Date - Feb 18, 2000
The date Desmopressin Acetate Preservative Free 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 Desmopressin Acetate Preservative Free. 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 Desmopressin Acetate Preservative Free is in. Format is RX, OTC, DISCN.

Applicant Full Name - Bedford Laboratories Div Ben Venue Laboratories Inc
The full name of the firm holding legal responsibility for the new application of Desmopressin Acetate Preservative Free.

Desmopressin Acetate Preservative Free