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