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hydroxyzine pamoate - 0185-0615-10 - (hydroxyzine pamoate)

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Drug Information of hydroxyzine pamoate

Product NDC: 0185-0615
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)

Labeler Information of hydroxyzine pamoate

Product NDC: 0185-0615
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086183
Marketing Category: ANDA
Start Marketing Date: 19811214

Package Information of hydroxyzine pamoate

Package NDC: 0185-0615-10
Package Description: 1000 CAPSULE in 1 BOTTLE (0185-0615-10)

NDC Information of hydroxyzine pamoate

NDC Code 0185-0615-10
Proprietary Name hydroxyzine pamoate
Package Description 1000 CAPSULE in 1 BOTTLE (0185-0615-10)
Product NDC 0185-0615
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 Eon Labs, Inc.
Substance Name HYDROXYZINE PAMOATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of hydroxyzine pamoate


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