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hydroxyzine pamoate
hydroxyzine pamoate - 0615-0331-39 - (hydroxyzine pamoate)
Drug Information of hydroxyzine pamoate
| Product NDC: | 0615-0331 |
| Proprietary Name: | hydroxyzine pamoate |
| Non Proprietary Name: | hydroxyzine pamoate |
| Active Ingredient(s): | 25 mg/1 & nbsp; hydroxyzine pamoate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of hydroxyzine pamoate
| Product NDC: | 0615-0331 |
| Labeler Name: | NCS HealthCare of KY, Inc dba Vangard Labs |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA087479 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19811214 |
Package Information of hydroxyzine pamoate
| Package NDC: | 0615-0331-39 |
| Package Description: | 30 CAPSULE in 1 BLISTER PACK (0615-0331-39) |
NDC Information of hydroxyzine pamoate
| NDC Code | 0615-0331-39 |
| Proprietary Name | hydroxyzine pamoate |
| Package Description | 30 CAPSULE in 1 BLISTER PACK (0615-0331-39) |
| Product NDC | 0615-0331 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | hydroxyzine pamoate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19811214 |
| Marketing Category Name | ANDA |
| Labeler Name | NCS HealthCare of KY, Inc dba Vangard Labs |
| Substance Name | HYDROXYZINE PAMOATE |
| Strength Number | 25 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |
