Home
>
National Drug Code (NDC)
>
Alprazolam
Alprazolam - 67296-0529-1 - (Alprazolam)
Drug Information of Alprazolam
| Product NDC: | 67296-0529 |
| 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) |
Labeler Information of Alprazolam
| Product NDC: | 67296-0529 |
| Labeler Name: | RedPharm |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074112 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080601 |
Package Information of Alprazolam
| Package NDC: | 67296-0529-1 |
| Package Description: | 20 TABLET in 1 BOTTLE (67296-0529-1) |
NDC Information of Alprazolam
| NDC Code | 67296-0529-1 |
| Proprietary Name | Alprazolam |
| Package Description | 20 TABLET in 1 BOTTLE (67296-0529-1) |
| Product NDC | 67296-0529 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Alprazolam |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080601 |
| Marketing Category Name | ANDA |
| Labeler Name | RedPharm |
| Substance Name | ALPRAZOLAM |
| Strength Number | .5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
