Home > National Drug Code (NDC) > Sunmark All Day Allergy D

Sunmark All Day Allergy D - 49348-851-04 - (Cetirizine HCl, Pseudoephedrine HCl)

Alphabetical Index


Drug Information of Sunmark All Day Allergy D

Product NDC: 49348-851
Proprietary Name: Sunmark All Day Allergy 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 Sunmark All Day Allergy D

Product NDC: 49348-851
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077170
Marketing Category: ANDA
Start Marketing Date: 20080418

Package Information of Sunmark All Day Allergy D

Package NDC: 49348-851-04
Package Description: 4 BLISTER PACK in 1 CARTON (49348-851-04) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Sunmark All Day Allergy D

NDC Code 49348-851-04
Proprietary Name Sunmark All Day Allergy D
Package Description 4 BLISTER PACK in 1 CARTON (49348-851-04) > 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 49348-851
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 20080418
Marketing Category Name ANDA
Labeler Name McKesson
Substance Name CETIRIZINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 5; 120
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Sunmark All Day Allergy D


General Information