Home
>
National Drug Code (NDC)
>
Alprazolam
Alprazolam - 0904-5861-61 - (Alprazolam)
Drug Information of Alprazolam
| Product NDC: | 0904-5861 |
| Proprietary Name: | Alprazolam |
| Non Proprietary Name: | Alprazolam |
| Active Ingredient(s): | 2 mg/1 & nbsp; Alprazolam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alprazolam
| Product NDC: | 0904-5861 |
| Labeler Name: | Major Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074342 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080402 |
Package Information of Alprazolam
| Package NDC: | 0904-5861-61 |
| Package Description: | 100 TABLET in 1 BOX, UNIT-DOSE (0904-5861-61) |
NDC Information of Alprazolam
| NDC Code | 0904-5861-61 |
| Proprietary Name | Alprazolam |
| Package Description | 100 TABLET in 1 BOX, UNIT-DOSE (0904-5861-61) |
| Product NDC | 0904-5861 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Alprazolam |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080402 |
| Marketing Category Name | ANDA |
| Labeler Name | Major Pharmaceuticals |
| Substance Name | ALPRAZOLAM |
| Strength Number | 2 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
