Alprazolam - 35356-504-90 - (alprazolam)

Alphabetical Index


Drug Information of Alprazolam

Product NDC: 35356-504
Proprietary Name: Alprazolam
Non Proprietary Name: alprazolam
Active Ingredient(s): 2    mg/1 & nbsp;   alprazolam
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Alprazolam

Product NDC: 35356-504
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021434
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20030117

Package Information of Alprazolam

Package NDC: 35356-504-90
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (35356-504-90)

NDC Information of Alprazolam

NDC Code 35356-504-90
Proprietary Name Alprazolam
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (35356-504-90)
Product NDC 35356-504
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprazolam
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030117
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name ALPRAZOLAM
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient]

Complete Information of Alprazolam


General Information