Etomidate - 67457-183-10 - (etomidate)

Alphabetical Index


Drug Information of Etomidate

Product NDC: 67457-183
Proprietary Name: Etomidate
Non Proprietary Name: etomidate
Active Ingredient(s): 2    mg/mL & nbsp;   etomidate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Etomidate

Product NDC: 67457-183
Labeler Name: Mylan Institutional LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091297
Marketing Category: ANDA
Start Marketing Date: 20130426

Package Information of Etomidate

Package NDC: 67457-183-10
Package Description: 10 VIAL, SINGLE-USE in 1 CARTON (67457-183-10) > 10 mL in 1 VIAL, SINGLE-USE (67457-183-00)

NDC Information of Etomidate

NDC Code 67457-183-10
Proprietary Name Etomidate
Package Description 10 VIAL, SINGLE-USE in 1 CARTON (67457-183-10) > 10 mL in 1 VIAL, SINGLE-USE (67457-183-00)
Product NDC 67457-183
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name etomidate
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20130426
Marketing Category Name ANDA
Labeler Name Mylan Institutional LLC
Substance Name ETOMIDATE
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes General Anesthesia [PE],General Anesthetic [EPC]

Complete Information of Etomidate


General Information