Product NDC: | 0009-0029 |
Proprietary Name: | Xanax |
Non Proprietary Name: | ALPRAZOLAM |
Active Ingredient(s): | .25 mg/1 & nbsp; ALPRAZOLAM |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0009-0029 |
Labeler Name: | Pharmacia and Upjohn Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA018276 |
Marketing Category: | NDA |
Start Marketing Date: | 19811016 |
Package NDC: | 0009-0029-01 |
Package Description: | 100 TABLET in 1 BOTTLE (0009-0029-01) |
NDC Code | 0009-0029-01 |
Proprietary Name | Xanax |
Package Description | 100 TABLET in 1 BOTTLE (0009-0029-01) |
Product NDC | 0009-0029 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ALPRAZOLAM |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19811016 |
Marketing Category Name | NDA |
Labeler Name | Pharmacia and Upjohn Company |
Substance Name | ALPRAZOLAM |
Strength Number | .25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |