Midazolam - 65293-417-25 - (MIDAZOLAM HYDROCHLORIDE)

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Drug Information of Midazolam

Product NDC: 65293-417
Proprietary Name: Midazolam
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

Product NDC: 65293-417
Labeler Name: The Medicines Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075154
Marketing Category: ANDA
Start Marketing Date: 20000714

Package Information of Midazolam

Package NDC: 65293-417-25
Package Description: 25 VIAL in 1 TRAY (65293-417-25) > 1 mL in 1 VIAL (65293-417-01)

NDC Information of Midazolam

NDC Code 65293-417-25
Proprietary Name Midazolam
Package Description 25 VIAL in 1 TRAY (65293-417-25) > 1 mL in 1 VIAL (65293-417-01)
Product NDC 65293-417
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MIDAZOLAM HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20000714
Marketing Category Name ANDA
Labeler Name The Medicines Company
Substance Name MIDAZOLAM HYDROCHLORIDE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Midazolam


General Information