Midazolam - 17478-523-02 - (Midazolam Hydrochloride)

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Drug Information of Midazolam

Product NDC: 17478-523
Proprietary Name: Midazolam
Non Proprietary Name: Midazolam Hydrochloride
Active Ingredient(s): 1    mg/mL & nbsp;   Midazolam Hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Midazolam

Product NDC: 17478-523
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075494
Marketing Category: ANDA
Start Marketing Date: 20050506

Package Information of Midazolam

Package NDC: 17478-523-02
Package Description: 10 VIAL in 1 CARTON (17478-523-02) > 2 mL in 1 VIAL

NDC Information of Midazolam

NDC Code 17478-523-02
Proprietary Name Midazolam
Package Description 10 VIAL in 1 CARTON (17478-523-02) > 2 mL in 1 VIAL
Product NDC 17478-523
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Midazolam Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20050506
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name MIDAZOLAM HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Midazolam


General Information