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Vistaril
Vistaril - 52125-001-08 - (hydroxyzine pamoate)
Drug Information of Vistaril
| Product NDC: | 52125-001 |
| Proprietary Name: | Vistaril |
| Non Proprietary Name: | hydroxyzine pamoate |
| Active Ingredient(s): | 50 mg/1 & nbsp; hydroxyzine pamoate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Vistaril
| Product NDC: | 52125-001 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA011459 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130311 |
Package Information of Vistaril
| Package NDC: | 52125-001-08 |
| Package Description: | 30 CAPSULE in 1 VIAL (52125-001-08) |
NDC Information of Vistaril
| NDC Code | 52125-001-08 |
| Proprietary Name | Vistaril |
| Package Description | 30 CAPSULE in 1 VIAL (52125-001-08) |
| Product NDC | 52125-001 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydroxyzine pamoate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130311 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | HYDROXYZINE PAMOATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
