| Product NDC: | 0054-3068 |
| Proprietary Name: | Alprazolam |
| Non Proprietary Name: | Alprazolam |
| Active Ingredient(s): | 1 mg/mL & nbsp; Alprazolam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION, CONCENTRATE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0054-3068 |
| Labeler Name: | Roxane Laboratories, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074312 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19931031 |
| Package NDC: | 0054-3068-44 |
| Package Description: | 1 BOTTLE in 1 CONTAINER (0054-3068-44) > 30 mL in 1 BOTTLE |
| NDC Code | 0054-3068-44 |
| Proprietary Name | Alprazolam |
| Package Description | 1 BOTTLE in 1 CONTAINER (0054-3068-44) > 30 mL in 1 BOTTLE |
| Product NDC | 0054-3068 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Alprazolam |
| Dosage Form Name | SOLUTION, CONCENTRATE |
| Route Name | ORAL |
| Start Marketing Date | 19931031 |
| Marketing Category Name | ANDA |
| Labeler Name | Roxane Laboratories, Inc |
| Substance Name | ALPRAZOLAM |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |