CETIRI D - 11822-0176-1 - (Cetirizine HCl, Pseudoephedrine HCl)

Alphabetical Index


Drug Information of CETIRI D

Product NDC: 11822-0176
Proprietary Name: CETIRI D
Non Proprietary Name: Cetirizine HCl, Pseudoephedrine HCl
Active Ingredient(s): 5; 120    mg/1; mg/1 & nbsp;   Cetirizine HCl, Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of CETIRI D

Product NDC: 11822-0176
Labeler Name: Rite Aid Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077170
Marketing Category: ANDA
Start Marketing Date: 20080410

Package Information of CETIRI D

Package NDC: 11822-0176-1
Package Description: 2 BLISTER PACK in 1 CARTON (11822-0176-1) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of CETIRI D

NDC Code 11822-0176-1
Proprietary Name CETIRI D
Package Description 2 BLISTER PACK in 1 CARTON (11822-0176-1) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 11822-0176
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Cetirizine HCl, Pseudoephedrine HCl
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20080410
Marketing Category Name ANDA
Labeler Name Rite Aid Corporation
Substance Name CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of CETIRI D


General Information