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Hydroxyzine Hydrochloride - 49349-648-31 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 49349-648
Proprietary Name: Hydroxyzine Hydrochloride
Non Proprietary Name: Hydroxyzine Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Hydroxyzine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxyzine Hydrochloride

Product NDC: 49349-648
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040804
Marketing Category: ANDA
Start Marketing Date: 20110523

Package Information of Hydroxyzine Hydrochloride

Package NDC: 49349-648-31
Package Description: 500 TABLET in 1 CANISTER (49349-648-31)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 49349-648-31
Proprietary Name Hydroxyzine Hydrochloride
Package Description 500 TABLET in 1 CANISTER (49349-648-31)
Product NDC 49349-648
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110523
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Hydrochloride


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