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Midazolam Hydrochloride - 55390-125-10 - (Midazolam Hydrochloride)

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Drug Information of Midazolam Hydrochloride

Product NDC: 55390-125
Proprietary Name: Midazolam Hydrochloride
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 Hydrochloride

Product NDC: 55390-125
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075421
Marketing Category: ANDA
Start Marketing Date: 20000621

Package Information of Midazolam Hydrochloride

Package NDC: 55390-125-10
Package Description: 10 VIAL in 1 BOX (55390-125-10) > 10 mL in 1 VIAL

NDC Information of Midazolam Hydrochloride

NDC Code 55390-125-10
Proprietary Name Midazolam Hydrochloride
Package Description 10 VIAL in 1 BOX (55390-125-10) > 10 mL in 1 VIAL
Product NDC 55390-125
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 Bedford Laboratories
Substance Name MIDAZOLAM HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Midazolam Hydrochloride


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