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Robitussin Maximum Strength Nighttime Cough DM
Robitussin Maximum Strength Nighttime Cough DM - 0031-8717-12 - (DEXTROMETHORPHAN HYDROBROMIDE and DOXYLAMINE SUCCINATE)
Drug Information of Robitussin Maximum Strength Nighttime Cough DM
| Product NDC: | 0031-8717 |
| Proprietary Name: | Robitussin Maximum Strength Nighttime Cough DM |
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE and DOXYLAMINE SUCCINATE |
| Active Ingredient(s): | 30; 12.5 mg/10mL; mg/10mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE and DOXYLAMINE SUCCINATE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Robitussin Maximum Strength Nighttime Cough DM
| Product NDC: | 0031-8717 |
| Labeler Name: | Richmond Division of Wyeth |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130301 |
Package Information of Robitussin Maximum Strength Nighttime Cough DM
| Package NDC: | 0031-8717-12 |
| Package Description: | 1 BOTTLE in 1 CARTON (0031-8717-12) > 118 mL in 1 BOTTLE |
NDC Information of Robitussin Maximum Strength Nighttime Cough DM
| NDC Code | 0031-8717-12 |
| Proprietary Name | Robitussin Maximum Strength Nighttime Cough DM |
| Package Description | 1 BOTTLE in 1 CARTON (0031-8717-12) > 118 mL in 1 BOTTLE |
| Product NDC | 0031-8717 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE and DOXYLAMINE SUCCINATE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20130301 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Richmond Division of Wyeth |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE |
| Strength Number | 30; 12.5 |
| Strength Unit | mg/10mL; mg/10mL |
| Pharmaceutical Classes |
