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Midazolam Hydrochloride - 54569-5255-1 - (MIDAZOLAM HYDROCHLORIDE)

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Drug Information of Midazolam Hydrochloride

Product NDC: 54569-5255
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, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Midazolam Hydrochloride

Product NDC: 54569-5255
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075293
Marketing Category: ANDA
Start Marketing Date: 20000620

Package Information of Midazolam Hydrochloride

Package NDC: 54569-5255-1
Package Description: 10 mL in 1 VIAL (54569-5255-1)

NDC Information of Midazolam Hydrochloride

NDC Code 54569-5255-1
Proprietary Name Midazolam Hydrochloride
Package Description 10 mL in 1 VIAL (54569-5255-1)
Product NDC 54569-5255
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 A-S Medication Solutions LLC
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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