Droperidol - 0409-1187-01 - (DROPERIDOL)

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Drug Information of Droperidol

Product NDC: 0409-1187
Proprietary Name: Droperidol
Non Proprietary Name: DROPERIDOL
Active Ingredient(s): 2.5    mg/mL & nbsp;   DROPERIDOL
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Droperidol

Product NDC: 0409-1187
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071981
Marketing Category: ANDA
Start Marketing Date: 20110811

Package Information of Droperidol

Package NDC: 0409-1187-01
Package Description: 10 AMPULE in 1 CARTON (0409-1187-01) > 2 mL in 1 AMPULE

NDC Information of Droperidol

NDC Code 0409-1187-01
Proprietary Name Droperidol
Package Description 10 AMPULE in 1 CARTON (0409-1187-01) > 2 mL in 1 AMPULE
Product NDC 0409-1187
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DROPERIDOL
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110811
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name DROPERIDOL
Strength Number 2.5
Strength Unit mg/mL
Pharmaceutical Classes Dopamine D2 Antagonists [MoA],Dopamine-2 Receptor Antagonist [EPC]

Complete Information of Droperidol


General Information