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Scot-Tussin Senior SF DMEXP
Scot-Tussin Senior SF DMEXP - 0372-0050-04 - (Dextromethorphan Hydrobromide, Guaifenesin)
Drug Information of Scot-Tussin Senior SF DMEXP
| Product NDC: | 0372-0050 |
| Proprietary Name: | Scot-Tussin Senior SF DMEXP |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Guaifenesin |
| Active Ingredient(s): | 15; 200 mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Scot-Tussin Senior SF DMEXP
| Product NDC: | 0372-0050 |
| Labeler Name: | SCOT-TUSSIN Pharmacal Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 19991207 |
Package Information of Scot-Tussin Senior SF DMEXP
| Package NDC: | 0372-0050-04 |
| Package Description: | 118 mL in 1 BOTTLE (0372-0050-04) |
NDC Information of Scot-Tussin Senior SF DMEXP
| NDC Code | 0372-0050-04 |
| Proprietary Name | Scot-Tussin Senior SF DMEXP |
| Package Description | 118 mL in 1 BOTTLE (0372-0050-04) |
| Product NDC | 0372-0050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 19991207 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | SCOT-TUSSIN Pharmacal Co., Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 15; 200 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
