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Leader TabTussin DM
Leader TabTussin DM - 37205-675-62 - (Dextromethorphan Hydrobromide / Guaifenesin)
Drug Information of Leader TabTussin DM
| Product NDC: | 37205-675 |
| Proprietary Name: | Leader TabTussin DM |
| Non Proprietary Name: | Dextromethorphan Hydrobromide / Guaifenesin |
| Active Ingredient(s): | 20; 400 mg/1; mg/1 & nbsp; Dextromethorphan Hydrobromide / Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Leader TabTussin DM
| Product NDC: | 37205-675 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120801 |
Package Information of Leader TabTussin DM
| Package NDC: | 37205-675-62 |
| Package Description: | 12 TABLET in 1 BLISTER PACK (37205-675-62) |
NDC Information of Leader TabTussin DM
| NDC Code | 37205-675-62 |
| Proprietary Name | Leader TabTussin DM |
| Package Description | 12 TABLET in 1 BLISTER PACK (37205-675-62) |
| Product NDC | 37205-675 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide / Guaifenesin |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120801 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Cardinal Health |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 20; 400 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
