Midazolam - 63323-412-05 - (MIDAZOLAM HYDROCHLORIDE)

Alphabetical Index


Drug Information of Midazolam

Product NDC: 63323-412
Proprietary Name: Midazolam
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

Product NDC: 63323-412
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075154
Marketing Category: ANDA
Start Marketing Date: 20000710

Package Information of Midazolam

Package NDC: 63323-412-05
Package Description: 10 VIAL in 1 TRAY (63323-412-05) > 5 mL in 1 VIAL

NDC Information of Midazolam

NDC Code 63323-412-05
Proprietary Name Midazolam
Package Description 10 VIAL in 1 TRAY (63323-412-05) > 5 mL in 1 VIAL
Product NDC 63323-412
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MIDAZOLAM HYDROCHLORIDE
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20000710
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name MIDAZOLAM HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Midazolam


General Information