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Cetirizine HCl and Pseudoephedrine HCl - 54868-5884-1 - (Cetirizine HCl and Pseudoephedrine HCl)

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Drug Information of Cetirizine HCl and Pseudoephedrine HCl

Product NDC: 54868-5884
Proprietary Name: Cetirizine HCl and Pseudoephedrine HCl
Non Proprietary Name: Cetirizine HCl and Pseudoephedrine HCl
Active Ingredient(s): 5; 120    mg/1; mg/1 & nbsp;   Cetirizine HCl and Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Cetirizine HCl and Pseudoephedrine HCl

Product NDC: 54868-5884
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077991
Marketing Category: ANDA
Start Marketing Date: 20080331

Package Information of Cetirizine HCl and Pseudoephedrine HCl

Package NDC: 54868-5884-1
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-5884-1)

NDC Information of Cetirizine HCl and Pseudoephedrine HCl

NDC Code 54868-5884-1
Proprietary Name Cetirizine HCl and Pseudoephedrine HCl
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (54868-5884-1)
Product NDC 54868-5884
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine HCl and Pseudoephedrine HCl
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080331
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Cetirizine HCl and Pseudoephedrine HCl


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