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