Lorazepam - 17478-040-01 - (Lorazepam)

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Drug Information of Lorazepam

Product NDC: 17478-040
Proprietary Name: Lorazepam
Non Proprietary Name: Lorazepam
Active Ingredient(s): 2    mg/mL & nbsp;   Lorazepam
Administration Route(s): INTRAMUSCULAR
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Lorazepam

Product NDC: 17478-040
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075025
Marketing Category: ANDA
Start Marketing Date: 19800701

Package Information of Lorazepam

Package NDC: 17478-040-01
Package Description: 10 VIAL in 1 CARTON (17478-040-01) > 1 mL in 1 VIAL

NDC Information of Lorazepam

NDC Code 17478-040-01
Proprietary Name Lorazepam
Package Description 10 VIAL in 1 CARTON (17478-040-01) > 1 mL in 1 VIAL
Product NDC 17478-040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR
Start Marketing Date 19800701
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name LORAZEPAM
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information