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Guaifenesin Phenylephrine Dextromethorphan
Guaifenesin Phenylephrine Dextromethorphan - 52083-249-60 - (Guaifenesin, phenylephrine HCL, Dextromethorphan)
Drug Information of Guaifenesin Phenylephrine Dextromethorphan
| Product NDC: | 52083-249 |
| Proprietary Name: | Guaifenesin Phenylephrine Dextromethorphan |
| Non Proprietary Name: | Guaifenesin, phenylephrine HCL, Dextromethorphan |
| Active Ingredient(s): | 20; 400; 10 mg/1; mg/1; mg/1 & nbsp; Guaifenesin, phenylephrine HCL, Dextromethorphan |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Guaifenesin Phenylephrine Dextromethorphan
| Product NDC: | 52083-249 |
| Labeler Name: | Kramer Novis. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120718 |
Package Information of Guaifenesin Phenylephrine Dextromethorphan
| Package NDC: | 52083-249-60 |
| Package Description: | 60 TABLET, COATED in 1 BOTTLE (52083-249-60) |
NDC Information of Guaifenesin Phenylephrine Dextromethorphan
| NDC Code | 52083-249-60 |
| Proprietary Name | Guaifenesin Phenylephrine Dextromethorphan |
| Package Description | 60 TABLET, COATED in 1 BOTTLE (52083-249-60) |
| Product NDC | 52083-249 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, phenylephrine HCL, Dextromethorphan |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20120718 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kramer Novis. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 20; 400; 10 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
