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Ritussin DM
Ritussin DM - 53807-409-08 - (DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN)
Drug Information of Ritussin DM
| Product NDC: | 53807-409 |
| Proprietary Name: | Ritussin DM |
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ritussin DM
| Product NDC: | 53807-409 |
| Labeler Name: | Rij Pharmaceutical Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19990316 |
Package Information of Ritussin DM
| Package NDC: | 53807-409-08 |
| Package Description: | 236 mL in 1 BOTTLE (53807-409-08) |
NDC Information of Ritussin DM
| NDC Code | 53807-409-08 |
| Proprietary Name | Ritussin DM |
| Package Description | 236 mL in 1 BOTTLE (53807-409-08) |
| Product NDC | 53807-409 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19990316 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rij Pharmaceutical Corporation |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
