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) |
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 NDC: | 50383-062-06 |
Package Description: | 4 TRAY in 1 CASE (50383-062-06) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-062-05) > 5 mL in 1 CUP, UNIT-DOSE |
NDC Code | 50383-062-06 |
Proprietary Name | Dextromethorphan HBr and Guaifenesin |
Package Description | 4 TRAY in 1 CASE (50383-062-06) > 10 CUP, UNIT-DOSE in 1 TRAY (50383-062-05) > 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 |