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Hydroxyzine Pamoate - 24236-070-04 - (Hydroxyzine Pamoate)

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Drug Information of Hydroxyzine Pamoate

Product NDC: 24236-070
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: 24236-070
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040156
Marketing Category: ANDA
Start Marketing Date: 20130319

Package Information of Hydroxyzine Pamoate

Package NDC: 24236-070-04
Package Description: 14 CAPSULE in 1 BLISTER PACK (24236-070-04)

NDC Information of Hydroxyzine Pamoate

NDC Code 24236-070-04
Proprietary Name Hydroxyzine Pamoate
Package Description 14 CAPSULE in 1 BLISTER PACK (24236-070-04)
Product NDC 24236-070
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Pamoate
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130319
Marketing Category Name ANDA
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 Hydroxyzine Pamoate


General Information