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Hydroxyzine Hydrochloride - 49349-696-02 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 49349-696
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: 49349-696
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088618
Marketing Category: ANDA
Start Marketing Date: 20110330

Package Information of Hydroxyzine Hydrochloride

Package NDC: 49349-696-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-696-02)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 49349-696-02
Proprietary Name Hydroxyzine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-696-02)
Product NDC 49349-696
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110330
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


General Information