Lorazepam - 52125-329-02 - (Lorazepam)

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Drug Information of Lorazepam

Product NDC: 52125-329
Proprietary Name: Lorazepam
Non Proprietary Name: Lorazepam
Active Ingredient(s): 2    mg/1 & nbsp;   Lorazepam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lorazepam

Product NDC: 52125-329
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072928
Marketing Category: ANDA
Start Marketing Date: 20130508

Package Information of Lorazepam

Package NDC: 52125-329-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-329-02)

NDC Information of Lorazepam

NDC Code 52125-329-02
Proprietary Name Lorazepam
Package Description 30 TABLET in 1 BLISTER PACK (52125-329-02)
Product NDC 52125-329
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lorazepam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130508
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LORAZEPAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Lorazepam


General Information