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Midazolam Hydrochloride - 0409-2596-53 - (MIDAZOLAM HYDROCHLORIDE)

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Drug Information of Midazolam Hydrochloride

Product NDC: 0409-2596
Proprietary Name: Midazolam Hydrochloride
Non Proprietary Name: MIDAZOLAM HYDROCHLORIDE
Active Ingredient(s): 5    mg/mL & nbsp;   MIDAZOLAM HYDROCHLORIDE
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Midazolam Hydrochloride

Product NDC: 0409-2596
Labeler Name: Hospira, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075293
Marketing Category: ANDA
Start Marketing Date: 20000620

Package Information of Midazolam Hydrochloride

Package NDC: 0409-2596-53
Package Description: 10 VIAL in 1 CARTON (0409-2596-53) > 10 mL in 1 VIAL

NDC Information of Midazolam Hydrochloride

NDC Code 0409-2596-53
Proprietary Name Midazolam Hydrochloride
Package Description 10 VIAL in 1 CARTON (0409-2596-53) > 10 mL in 1 VIAL
Product NDC 0409-2596
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MIDAZOLAM HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20000620
Marketing Category Name ANDA
Labeler Name Hospira, Inc.
Substance Name MIDAZOLAM HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Midazolam Hydrochloride


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