Home
>
National Drug Code (NDC)
>
DICEL
DICEL - 11528-101-02 - (Chlorpheniramine/Pseudoephedrine)
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 |
