Product NDC: | 21695-605 |
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: | 21695-605 |
Labeler Name: | Rebel Distributors Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078387 |
Marketing Category: | ANDA |
Start Marketing Date: | 20091203 |
Package NDC: | 21695-605-60 |
Package Description: | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-605-60) |
NDC Code | 21695-605-60 |
Proprietary Name | Alprazolam |
Package Description | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-605-60) |
Product NDC | 21695-605 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Alprazolam |
Dosage Form Name | TABLET, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20091203 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp. |
Substance Name | ALPRAZOLAM |
Strength Number | 2 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |