Home
>
National Drug Code (NDC)
>
Robitussin Peak Cold Cough Plus Chest Congestion DM
Robitussin Peak Cold Cough Plus Chest Congestion DM - 0031-8736-42 - (DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN)
Drug Information of Robitussin Peak Cold Cough Plus Chest Congestion DM
| Product NDC: | 0031-8736 |
| Proprietary Name: | Robitussin Peak Cold Cough Plus Chest Congestion DM |
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Robitussin Peak Cold Cough Plus Chest Congestion DM
| Product NDC: | 0031-8736 |
| Labeler Name: | Richmond Division of Wyeth |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110615 |
Package Information of Robitussin Peak Cold Cough Plus Chest Congestion DM
| Package NDC: | 0031-8736-42 |
| Package Description: | 1 BOTTLE in 1 CARTON (0031-8736-42) > 355 mL in 1 BOTTLE |
NDC Information of Robitussin Peak Cold Cough Plus Chest Congestion DM
| NDC Code | 0031-8736-42 |
| Proprietary Name | Robitussin Peak Cold Cough Plus Chest Congestion DM |
| Package Description | 1 BOTTLE in 1 CARTON (0031-8736-42) > 355 mL in 1 BOTTLE |
| Product NDC | 0031-8736 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110615 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Richmond Division of Wyeth |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 100 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes |
