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] |