MIDAZOLAM - 57664-633-43 - (MIDAZOLAM HYDROCHLORIDE)

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Drug Information of MIDAZOLAM

Product NDC: 57664-633
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
Coding System: National Drug Codes(NDC)

Labeler Information of MIDAZOLAM

Product NDC: 57664-633
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090696
Marketing Category: ANDA
Start Marketing Date: 20120808

Package Information of MIDAZOLAM

Package NDC: 57664-633-43
Package Description: 10 VIAL in 1 CARTON (57664-633-43) > 2 mL in 1 VIAL (57664-633-40)

NDC Information of MIDAZOLAM

NDC Code 57664-633-43
Proprietary Name MIDAZOLAM
Package Description 10 VIAL in 1 CARTON (57664-633-43) > 2 mL in 1 VIAL (57664-633-40)
Product NDC 57664-633
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MIDAZOLAM HYDROCHLORIDE
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20120808
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd.
Substance Name MIDAZOLAM HYDROCHLORIDE
Strength Number 1
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of MIDAZOLAM


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