Alprazolam - 49999-252-90 - (Alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 49999-252
Proprietary Name: Alprazolam
Non Proprietary Name: Alprazolam
Active Ingredient(s): 1    mg/1 & nbsp;   Alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 49999-252
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018276
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20111130

Package Information of Alprazolam

Package NDC: 49999-252-90
Package Description: 90 TABLET in 1 BOTTLE (49999-252-90)

NDC Information of Alprazolam

NDC Code 49999-252-90
Proprietary Name Alprazolam
Package Description 90 TABLET in 1 BOTTLE (49999-252-90)
Product NDC 49999-252
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Alprazolam
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111130
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name ALPRAZOLAM
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information