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Pedia Relief
Pedia Relief - 0904-5050-20 - (Chlorpheniramine maleate and Pseudoephedrine hydrochloride and Dextromethorphan hydrobromide)
Drug Information of Pedia Relief
| Product NDC: | 0904-5050 |
| Proprietary Name: | Pedia Relief |
| Non Proprietary Name: | Chlorpheniramine maleate and Pseudoephedrine hydrochloride and Dextromethorphan hydrobromide |
| Active Ingredient(s): | 1; 5; 15 mg/5mL; mg/5mL; mg/5mL & nbsp; Chlorpheniramine maleate and Pseudoephedrine hydrochloride and Dextromethorphan hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Pedia Relief
| Product NDC: | 0904-5050 |
| Labeler Name: | Major Pharmaceuticals, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19970105 |
Package Information of Pedia Relief
| Package NDC: | 0904-5050-20 |
| Package Description: | 120 mL in 1 BOTTLE, PLASTIC (0904-5050-20) |
NDC Information of Pedia Relief
| NDC Code | 0904-5050-20 |
| Proprietary Name | Pedia Relief |
| Package Description | 120 mL in 1 BOTTLE, PLASTIC (0904-5050-20) |
| Product NDC | 0904-5050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Chlorpheniramine maleate and Pseudoephedrine hydrochloride and Dextromethorphan hydrobromide |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19970105 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Major Pharmaceuticals, Inc |
| Substance Name | CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 1; 5; 15 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
