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Hydroxyzine Hydrochloride - 21695-378-30 - (Hydroxyzine Hydrochloride)

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Drug Information of Hydroxyzine Hydrochloride

Product NDC: 21695-378
Proprietary Name: Hydroxyzine Hydrochloride
Non Proprietary Name: Hydroxyzine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Hydroxyzine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Hydroxyzine Hydrochloride

Product NDC: 21695-378
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040804
Marketing Category: ANDA
Start Marketing Date: 20080630

Package Information of Hydroxyzine Hydrochloride

Package NDC: 21695-378-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (21695-378-30)

NDC Information of Hydroxyzine Hydrochloride

NDC Code 21695-378-30
Proprietary Name Hydroxyzine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (21695-378-30)
Product NDC 21695-378
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydroxyzine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20080630
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
Substance Name HYDROXYZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Antihistamine [EPC],Histamine Receptor Antagonists [MoA]

Complete Information of Hydroxyzine Hydrochloride


General Information