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Poly-Vent DM
Poly-Vent DM - 50991-214-01 - (Dextromethorphan HBr, Guaifenesin and Pseudoephedrine HCl)
Drug Information of Poly-Vent DM
| Product NDC: | 50991-214 |
| Proprietary Name: | Poly-Vent DM |
| Non Proprietary Name: | Dextromethorphan HBr, Guaifenesin and Pseudoephedrine HCl |
| Active Ingredient(s): | 20; 380; 60 mg/1; mg/1; mg/1 & nbsp; Dextromethorphan HBr, Guaifenesin and Pseudoephedrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Poly-Vent DM
| Product NDC: | 50991-214 |
| Labeler Name: | Poly Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130617 |
Package Information of Poly-Vent DM
| Package NDC: | 50991-214-01 |
| Package Description: | 100 TABLET in 1 BOTTLE (50991-214-01) |
NDC Information of Poly-Vent DM
| NDC Code | 50991-214-01 |
| Proprietary Name | Poly-Vent DM |
| Package Description | 100 TABLET in 1 BOTTLE (50991-214-01) |
| Product NDC | 50991-214 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan HBr, Guaifenesin and Pseudoephedrine HCl |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20130617 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Poly Pharmaceuticals, Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Strength Number | 20; 380; 60 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
