| Product NDC: | 24236-070 |
| 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: | 24236-070 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA040156 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130319 |
| Package NDC: | 24236-070-04 |
| Package Description: | 14 CAPSULE in 1 BLISTER PACK (24236-070-04) |
| NDC Code | 24236-070-04 |
| Proprietary Name | Hydroxyzine Pamoate |
| Package Description | 14 CAPSULE in 1 BLISTER PACK (24236-070-04) |
| Product NDC | 24236-070 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Hydroxyzine Pamoate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130319 |
| Marketing Category Name | ANDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | HYDROXYZINE PAMOATE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |