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Childrens Mucinex
Childrens Mucinex - 63824-256-12 - (Guaifenesin and Dextromethorphan Hydrobromide)
Drug Information of Childrens Mucinex
| Product NDC: | 63824-256 |
| Proprietary Name: | Childrens Mucinex |
| Non Proprietary Name: | Guaifenesin and Dextromethorphan Hydrobromide |
| Active Ingredient(s): | 5; 100 mg/1; mg/1 & nbsp; Guaifenesin and Dextromethorphan Hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GRANULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Childrens Mucinex
| Product NDC: | 63824-256 |
| Labeler Name: | Reckitt Benckiser |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090324 |
Package Information of Childrens Mucinex
| Package NDC: | 63824-256-12 |
| Package Description: | 12 PACKET in 1 CARTON (63824-256-12) > 1 GRANULE in 1 PACKET |
NDC Information of Childrens Mucinex
| NDC Code | 63824-256-12 |
| Proprietary Name | Childrens Mucinex |
| Package Description | 12 PACKET in 1 CARTON (63824-256-12) > 1 GRANULE in 1 PACKET |
| Product NDC | 63824-256 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin and Dextromethorphan Hydrobromide |
| Dosage Form Name | GRANULE |
| Route Name | ORAL |
| Start Marketing Date | 20090324 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Reckitt Benckiser |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
| Strength Number | 5; 100 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
