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Dextromethorphan HBr and Guaifenesin
Dextromethorphan HBr and Guaifenesin - 50383-062-07 - (Dextromethorphan HBr and Guaifenesin)
Drug Information of Dextromethorphan HBr and Guaifenesin
| Product NDC: | 50383-062 |
| Proprietary Name: | Dextromethorphan HBr and Guaifenesin |
| Non Proprietary Name: | Dextromethorphan HBr and Guaifenesin |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; Dextromethorphan HBr and Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Dextromethorphan HBr and Guaifenesin
| Product NDC: | 50383-062 |
| Labeler Name: | Hi-Tech Pharmacal Co., Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120307 |
Package Information of Dextromethorphan HBr and Guaifenesin
| Package NDC: | 50383-062-07 |
| Package Description: | 10 TRAY in 1 CASE (50383-062-07) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE |
NDC Information of Dextromethorphan HBr and Guaifenesin
| NDC Code | 50383-062-07 |
| Proprietary Name | Dextromethorphan HBr and Guaifenesin |
| Package Description | 10 TRAY in 1 CASE (50383-062-07) > 10 CUP, UNIT-DOSE in 1 TRAY > 5 mL in 1 CUP, UNIT-DOSE |
| Product NDC | 50383-062 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan HBr and Guaifenesin |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20120307 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Hi-Tech Pharmacal Co., Inc. |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
