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Allfen DM
Allfen DM - 58605-401-01 - (GUAIFENESIN and Dextromethorphan Hydrobromide)
Drug Information of Allfen DM
| Product NDC: | 58605-401 |
| Proprietary Name: | Allfen DM |
| Non Proprietary Name: | GUAIFENESIN and Dextromethorphan Hydrobromide |
| Active Ingredient(s): | 20; 400 mg/1; mg/1 & nbsp; GUAIFENESIN and Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Allfen DM
| Product NDC: | 58605-401 |
| Labeler Name: | MCR American Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20080331 |
Package Information of Allfen DM
| Package NDC: | 58605-401-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (58605-401-01) |
NDC Information of Allfen DM
| NDC Code | 58605-401-01 |
| Proprietary Name | Allfen DM |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (58605-401-01) |
| Product NDC | 58605-401 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN and Dextromethorphan Hydrobromide |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20080331 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MCR American Pharmaceuticals, Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 20; 400 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
