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Codituss DM
Codituss DM - 0603-0728-54 - (dextromethorphan hydrobromide and phenylephrine hydrochloride and pyrilamine maleate)
Drug Information of Codituss DM
| Product NDC: | 0603-0728 |
| Proprietary Name: | Codituss DM |
| Non Proprietary Name: | dextromethorphan hydrobromide and phenylephrine hydrochloride and pyrilamine maleate |
| Active Ingredient(s): | 10; 5; 8.33 mg/5mL; mg/5mL; mg/5mL & nbsp; dextromethorphan hydrobromide and phenylephrine hydrochloride and pyrilamine maleate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Codituss DM
| Product NDC: | 0603-0728 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19971001 |
Package Information of Codituss DM
| Package NDC: | 0603-0728-54 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (0603-0728-54) |
NDC Information of Codituss DM
| NDC Code | 0603-0728-54 |
| Proprietary Name | Codituss DM |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (0603-0728-54) |
| Product NDC | 0603-0728 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan hydrobromide and phenylephrine hydrochloride and pyrilamine maleate |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 19971001 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE; PYRILAMINE MALEATE |
| Strength Number | 10; 5; 8.33 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
