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Midazolam Hydrochloride - 55154-0359-5 - (Midazolam Hydrochloride)

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Drug Information of Midazolam Hydrochloride

Product NDC: 55154-0359
Proprietary Name: Midazolam Hydrochloride
Non Proprietary Name: Midazolam Hydrochloride
Active Ingredient(s): 10    mg/2mL & nbsp;   Midazolam Hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Midazolam Hydrochloride

Product NDC: 55154-0359
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075421
Marketing Category: ANDA
Start Marketing Date: 20000621

Package Information of Midazolam Hydrochloride

Package NDC: 55154-0359-5
Package Description: 5 VIAL in 1 BAG (55154-0359-5) > 2 mL in 1 VIAL

NDC Information of Midazolam Hydrochloride

NDC Code 55154-0359-5
Proprietary Name Midazolam Hydrochloride
Package Description 5 VIAL in 1 BAG (55154-0359-5) > 2 mL in 1 VIAL
Product NDC 55154-0359
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Midazolam Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20000621
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name MIDAZOLAM HYDROCHLORIDE
Strength Number 10
Strength Unit mg/2mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Midazolam Hydrochloride


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