Home > National Drug Code (NDC) > hydroxyzine pamoate

hydroxyzine pamoate - 0615-0331-39 - (hydroxyzine pamoate)

Alphabetical Index


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]

Complete Information of hydroxyzine pamoate


General Information