Product NDC: | 43063-367 |
Proprietary Name: | Alprazolam |
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) |
Product NDC: | 43063-367 |
Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074174 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070328 |
Package NDC: | 43063-367-98 |
Package Description: | 120 TABLET in 1 BOTTLE, PLASTIC (43063-367-98) |
NDC Code | 43063-367-98 |
Proprietary Name | Alprazolam |
Package Description | 120 TABLET in 1 BOTTLE, PLASTIC (43063-367-98) |
Product NDC | 43063-367 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Alprazolam |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20070328 |
Marketing Category Name | ANDA |
Labeler Name | PD-Rx Pharmaceuticals, Inc. |
Substance Name | ALPRAZOLAM |
Strength Number | .5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |