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Rycontuss
Rycontuss - 76117-001-16 - (CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE)
Drug Information of Rycontuss
| Product NDC: | 76117-001 |
| Proprietary Name: | Rycontuss |
| Non Proprietary Name: | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 2; 10; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Rycontuss
| Product NDC: | 76117-001 |
| Labeler Name: | Okendpharma, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110531 |
Package Information of Rycontuss
| Package NDC: | 76117-001-16 |
| Package Description: | 473 mL in 1 BOTTLE (76117-001-16) |
NDC Information of Rycontuss
| NDC Code | 76117-001-16 |
| Proprietary Name | Rycontuss |
| Package Description | 473 mL in 1 BOTTLE (76117-001-16) |
| Product NDC | 76117-001 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CHLORPHENIRAMINE MALEATE, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110531 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Okendpharma, Inc. |
| Substance Name | CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 2; 10; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
