Product NDC: | 16590-938 |
Proprietary Name: | NIRAVAM |
Non Proprietary Name: | ALPRAZOLAM |
Active Ingredient(s): | .5 mg/1 & nbsp; ALPRAZOLAM |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-938 |
Labeler Name: | STAT RX USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021726 |
Marketing Category: | NDA |
Start Marketing Date: | 20050120 |
Package NDC: | 16590-938-90 |
Package Description: | 90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (16590-938-90) |
NDC Code | 16590-938-90 |
Proprietary Name | NIRAVAM |
Package Description | 90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (16590-938-90) |
Product NDC | 16590-938 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ALPRAZOLAM |
Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
Route Name | ORAL |
Start Marketing Date | 20050120 |
Marketing Category Name | NDA |
Labeler Name | STAT RX USA LLC |
Substance Name | ALPRAZOLAM |
Strength Number | .5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |