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Niravam
Niravam - 0091-3321-01 - (alprazolam)
Drug Information of Niravam
| Product NDC: | 0091-3321 |
| Proprietary Name: | Niravam |
| Non Proprietary Name: | alprazolam |
| Active Ingredient(s): | .25 mg/1 & nbsp; alprazolam |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Niravam
| Product NDC: | 0091-3321 |
| Labeler Name: | Schwarz Pharma Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021726 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20050120 |
Package Information of Niravam
| Package NDC: | 0091-3321-01 |
| Package Description: | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0091-3321-01) |
NDC Information of Niravam
| NDC Code | 0091-3321-01 |
| Proprietary Name | Niravam |
| Package Description | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (0091-3321-01) |
| Product NDC | 0091-3321 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | alprazolam |
| Dosage Form Name | TABLET, ORALLY DISINTEGRATING |
| Route Name | ORAL |
| Start Marketing Date | 20050120 |
| Marketing Category Name | NDA |
| Labeler Name | Schwarz Pharma Inc. |
| Substance Name | ALPRAZOLAM |
| Strength Number | .25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Benzodiazepine [EPC],Benzodiazepines [Chemical/Ingredient] |
