Product NDC: | 62584-739 |
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) |
Product NDC: | 62584-739 |
Labeler Name: | American Health Packaging |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA087479 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130612 |
Package NDC: | 62584-739-01 |
Package Description: | 10 BLISTER PACK in 1 CARTON (62584-739-01) > 10 CAPSULE in 1 BLISTER PACK (62584-739-11) |
NDC Code | 62584-739-01 |
Proprietary Name | hydroxyzine pamoate |
Package Description | 10 BLISTER PACK in 1 CARTON (62584-739-01) > 10 CAPSULE in 1 BLISTER PACK (62584-739-11) |
Product NDC | 62584-739 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | hydroxyzine pamoate |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20130612 |
Marketing Category Name | ANDA |
Labeler Name | American Health Packaging |
Substance Name | HYDROXYZINE PAMOATE |
Strength Number | 25 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Antihistamine [EPC],Histamine Receptor Antagonists [MoA] |