Lorazepam - 0121-0770-01 - (Lorazepam)

Alphabetical Index


Drug Information of Lorazepam

Product NDC: 0121-0770
Proprietary Name: Lorazepam
Non Proprietary Name: Lorazepam
Active Ingredient(s): 2    mg/mL & nbsp;   Lorazepam
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Lorazepam

Product NDC: 0121-0770
Labeler Name: Pharmaceutical Associates, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090260
Marketing Category: ANDA
Start Marketing Date: 20101101

Package Information of Lorazepam

Package NDC: 0121-0770-01
Package Description: 30 mL in 1 BOTTLE, DROPPER (0121-0770-01)

NDC Information of Lorazepam

NDC Code 0121-0770-01
Proprietary Name Lorazepam
Package Description 30 mL in 1 BOTTLE, DROPPER (0121-0770-01)
Product NDC 0121-0770
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20101101
Marketing Category Name ANDA
Labeler Name Pharmaceutical Associates, Inc.
Substance Name LORAZEPAM
Strength Number 2
Strength Unit mg/mL
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information