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ExeFen DMX
ExeFen DMX - 68047-155-01 - (Dextromethorphan Hydrobromide, Guaifenesin and Pseudoephedrine Hydrochloride)
Drug Information of ExeFen DMX
| Product NDC: | 68047-155 |
| Proprietary Name: | ExeFen DMX |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Guaifenesin and Pseudoephedrine Hydrochloride |
| Active Ingredient(s): | 20; 400; 60 mg/1; mg/1; mg/1 & nbsp; Dextromethorphan Hydrobromide, Guaifenesin and Pseudoephedrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ExeFen DMX
| Product NDC: | 68047-155 |
| Labeler Name: | Larken Laboratories, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110328 |
Package Information of ExeFen DMX
| Package NDC: | 68047-155-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (68047-155-01) |
NDC Information of ExeFen DMX
| NDC Code | 68047-155-01 |
| Proprietary Name | ExeFen DMX |
| Package Description | 100 TABLET in 1 BOTTLE (68047-155-01) |
| Product NDC | 68047-155 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin and Pseudoephedrine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20110328 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Larken Laboratories, Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 20; 400; 60 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
