Kidkare - 0536-2310-97 - (Chlorpheniramine, Dextromethorphan Hydrobromide, and Pseudoephedrine Hydrochloride)

Alphabetical Index


Drug Information of Kidkare

Product NDC: 0536-2310
Proprietary Name: Kidkare
Non Proprietary Name: Chlorpheniramine, Dextromethorphan Hydrobromide, and Pseudoephedrine Hydrochloride
Active Ingredient(s): 1; 5; 15    mg/5mL; mg/5mL; mg/5mL & nbsp;   Chlorpheniramine, Dextromethorphan Hydrobromide, and Pseudoephedrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Kidkare

Product NDC: 0536-2310
Labeler Name: Rugby Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110113

Package Information of Kidkare

Package NDC: 0536-2310-97
Package Description: 118 mL in 1 BOTTLE (0536-2310-97)

NDC Information of Kidkare

NDC Code 0536-2310-97
Proprietary Name Kidkare
Package Description 118 mL in 1 BOTTLE (0536-2310-97)
Product NDC 0536-2310
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Chlorpheniramine, Dextromethorphan Hydrobromide, and Pseudoephedrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110113
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Rugby Laboratories, Inc.
Substance Name CHLORPHENIRAMINE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 1; 5; 15
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Kidkare


General Information