DICEL - 11528-101-02 - (Chlorpheniramine/Pseudoephedrine)

Alphabetical Index


Drug Information of DICEL

Product NDC: 11528-101
Proprietary Name: DICEL
Non Proprietary Name: Chlorpheniramine/Pseudoephedrine
Active Ingredient(s): 2; 30    mg/1; mg/1 & nbsp;   Chlorpheniramine/Pseudoephedrine
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of DICEL

Product NDC: 11528-101
Labeler Name: Centrix Pharmaceutical
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20100930

Package Information of DICEL

Package NDC: 11528-101-02
Package Description: 20 TABLET, CHEWABLE in 1 CARTON (11528-101-02)

NDC Information of DICEL

NDC Code 11528-101-02
Proprietary Name DICEL
Package Description 20 TABLET, CHEWABLE in 1 CARTON (11528-101-02)
Product NDC 11528-101
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Chlorpheniramine/Pseudoephedrine
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20100930
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Centrix Pharmaceutical
Substance Name CHLORPHENIRAMINE MALEATE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 2; 30
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of DICEL


General Information