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Mucus Relief Cough
Mucus Relief Cough - 11822-0533-3 - (Guaifenesin and Dextromethorphan HBr)
Drug Information of Mucus Relief Cough
| Product NDC: | 11822-0533 |
| Proprietary Name: | Mucus Relief Cough |
| Non Proprietary Name: | Guaifenesin and Dextromethorphan HBr |
| Active Ingredient(s): | 20; 400 mg/1; mg/1 & nbsp; Guaifenesin and Dextromethorphan HBr |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucus Relief Cough
| Product NDC: | 11822-0533 |
| Labeler Name: | Rite Aid |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20051231 |
Package Information of Mucus Relief Cough
| Package NDC: | 11822-0533-3 |
| Package Description: | 1 BLISTER PACK in 1 CARTON (11822-0533-3) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Mucus Relief Cough
| NDC Code | 11822-0533-3 |
| Proprietary Name | Mucus Relief Cough |
| Package Description | 1 BLISTER PACK in 1 CARTON (11822-0533-3) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 11822-0533 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin and Dextromethorphan HBr |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20051231 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Rite Aid |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 20; 400 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
