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Xanax
Xanax - 0009-0055-01 - (ALPRAZOLAM)
Drug Information of Xanax
| Product NDC: | 0009-0055 |
| Proprietary Name: | Xanax |
| Non Proprietary Name: | ALPRAZOLAM |
| Active Ingredient(s): | .5 mg/1 & nbsp; ALPRAZOLAM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Xanax
| Product NDC: | 0009-0055 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018276 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19811016 |
Package Information of Xanax
| Package NDC: | 0009-0055-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (0009-0055-01) |
NDC Information of Xanax
| NDC Code | 0009-0055-01 |
| Proprietary Name | Xanax |
| Package Description | 100 TABLET in 1 BOTTLE (0009-0055-01) |
| Product NDC | 0009-0055 |
| 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 | .5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
