Vistaril - 52125-001-08 - (hydroxyzine pamoate)

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Drug Information of Vistaril

Product NDC: 52125-001
Proprietary Name: Vistaril
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)

Labeler Information of Vistaril

Product NDC: 52125-001
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA011459
Marketing Category: NDA
Start Marketing Date: 20130311

Package Information of Vistaril

Package NDC: 52125-001-08
Package Description: 30 CAPSULE in 1 VIAL (52125-001-08)

NDC Information of Vistaril

NDC Code 52125-001-08
Proprietary Name Vistaril
Package Description 30 CAPSULE in 1 VIAL (52125-001-08)
Product NDC 52125-001
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name hydroxyzine pamoate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130311
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name HYDROXYZINE PAMOATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Vistaril


General Information