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Robitussin Maximum Strength Cough plus Chest Congestion DM
Robitussin Maximum Strength Cough plus Chest Congestion DM - 0031-8719-20 - (DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN)
Drug Information of Robitussin Maximum Strength Cough plus Chest Congestion DM
| Product NDC: | 0031-8719 |
| Proprietary Name: | Robitussin Maximum Strength Cough plus Chest Congestion DM |
| Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Active Ingredient(s): | 10; 200 mg/1; mg/1 & nbsp; DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Robitussin Maximum Strength Cough plus Chest Congestion DM
| Product NDC: | 0031-8719 |
| Labeler Name: | Richmond Division of Wyeth |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130523 |
Package Information of Robitussin Maximum Strength Cough plus Chest Congestion DM
| Package NDC: | 0031-8719-20 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0031-8719-20) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Information of Robitussin Maximum Strength Cough plus Chest Congestion DM
| NDC Code | 0031-8719-20 |
| Proprietary Name | Robitussin Maximum Strength Cough plus Chest Congestion DM |
| Package Description | 2 BLISTER PACK in 1 CARTON (0031-8719-20) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
| Product NDC | 0031-8719 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20130523 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Richmond Division of Wyeth |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 10; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
