| Product NDC: | 64980-170 |
| Proprietary Name: | HYDROXYZINE PAMOATE |
| 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) |
| Product NDC: | 64980-170 |
| Labeler Name: | Rising Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA201507 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101117 |
| Package NDC: | 64980-170-05 |
| Package Description: | 500 CAPSULE in 1 CONTAINER (64980-170-05) |
| NDC Code | 64980-170-05 |
| Proprietary Name | HYDROXYZINE PAMOATE |
| Package Description | 500 CAPSULE in 1 CONTAINER (64980-170-05) |
| Product NDC | 64980-170 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | HYDROXYZINE PAMOATE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20101117 |
| Marketing Category Name | ANDA |
| Labeler Name | Rising Pharmaceuticals Inc. |
| Substance Name | HYDROXYZINE PAMOATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |