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] |