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adult severe congestion and cough
adult severe congestion and cough - 49348-083-36 - (Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl)
Drug Information of adult severe congestion and cough
| Product NDC: | 49348-083 |
| Proprietary Name: | adult severe congestion and cough |
| Non Proprietary Name: | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Active Ingredient(s): | 20; 400; 10 mg/20mL; mg/20mL; mg/20mL & nbsp; Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of adult severe congestion and cough
| Product NDC: | 49348-083 |
| Labeler Name: | Mckesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20121201 |
Package Information of adult severe congestion and cough
| Package NDC: | 49348-083-36 |
| Package Description: | 177 mL in 1 BOTTLE (49348-083-36) |
NDC Information of adult severe congestion and cough
| NDC Code | 49348-083-36 |
| Proprietary Name | adult severe congestion and cough |
| Package Description | 177 mL in 1 BOTTLE (49348-083-36) |
| Product NDC | 49348-083 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20121201 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Mckesson |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 20; 400; 10 |
| Strength Unit | mg/20mL; mg/20mL; mg/20mL |
| Pharmaceutical Classes |
