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DECONEX
DECONEX - 50991-730-60 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)
Drug Information of DECONEX
| Product NDC: | 50991-730 |
| Proprietary Name: | DECONEX |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Active Ingredient(s): | 15; 380; 10 mg/1; mg/1; mg/1 & nbsp; Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DECONEX
| Product NDC: | 50991-730 |
| Labeler Name: | Poly Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120217 |
Package Information of DECONEX
| Package NDC: | 50991-730-60 |
| Package Description: | 60 TABLET in 1 BOTTLE (50991-730-60) |
NDC Information of DECONEX
| NDC Code | 50991-730-60 |
| Proprietary Name | DECONEX |
| Package Description | 60 TABLET in 1 BOTTLE (50991-730-60) |
| Product NDC | 50991-730 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20120217 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Poly Pharmaceuticals |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 15; 380; 10 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
