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GUAIFENESIN DM
GUAIFENESIN DM - 68752-012-90 - (GUAIFENESIN DEXTROMETHORPHAN)
Drug Information of GUAIFENESIN DM
| Product NDC: | 68752-012 |
| Proprietary Name: | GUAIFENESIN DM |
| Non Proprietary Name: | GUAIFENESIN DEXTROMETHORPHAN |
| Active Ingredient(s): | 20; 400 mg/1; mg/1 & nbsp; GUAIFENESIN DEXTROMETHORPHAN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GUAIFENESIN DM
| Product NDC: | 68752-012 |
| Labeler Name: | PD-Rx Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120417 |
Package Information of GUAIFENESIN DM
| Package NDC: | 68752-012-90 |
| Package Description: | 90 TABLET in 1 BOTTLE, PLASTIC (68752-012-90) |
NDC Information of GUAIFENESIN DM
| NDC Code | 68752-012-90 |
| Proprietary Name | GUAIFENESIN DM |
| Package Description | 90 TABLET in 1 BOTTLE, PLASTIC (68752-012-90) |
| Product NDC | 68752-012 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | GUAIFENESIN DEXTROMETHORPHAN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120417 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | PD-Rx Pharmaceuticals, Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 20; 400 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
