Fentanyl Citrate And Droperidol

   
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Fentanyl Citrate And Droperidol


Drug - Fentanyl Citrate And Droperidol
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) - Droperidol; Fentanyl Citrate
Multiple ingredients are in alphabetical order.

Strength - 2.5MG/ML;EQ 0.05MG BASE/ML
The potency of the active ingredient(s), Droperidol; Fentanyl Citrate. May repeat for multiple part products.

Applicant - HOSPIRA
The firm name holding legal responsibility for Fentanyl Citrate And Droperidol. The firm name is condensed to a maximum twenty character unique string.

New Drug Application (NDA) Number - 071982
The FDA assigned number to Fentanyl Citrate And Droperidol. Format is nnnnnn.

Product Number - 001
The FDA assigned number to identify Fentanyl Citrate And Droperidol. 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 - May 4, 1988
The date Fentanyl Citrate And Droperidol 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 Fentanyl Citrate And Droperidol. 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 Fentanyl Citrate And Droperidol is in. Format is RX, OTC, DISCN.

Applicant Full Name - Hospira Inc
The full name of the firm holding legal responsibility for the new application of Fentanyl Citrate And Droperidol.

Fentanyl Citrate And Droperidol