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Mucinex
Mucinex - 63824-273-64 - (Guaifenesin)
Drug Information of Mucinex
| Product NDC: | 63824-273 |
| Proprietary Name: | Mucinex |
| Non Proprietary Name: | Guaifenesin |
| Active Ingredient(s): | 100 mg/5mL & nbsp; Guaifenesin |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucinex
| Product NDC: | 63824-273 |
| Labeler Name: | Reckitt Benckiser, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090408 |
Package Information of Mucinex
| Package NDC: | 63824-273-64 |
| Package Description: | 1 BOTTLE in 1 CARTON (63824-273-64) > 118 mL in 1 BOTTLE |
NDC Information of Mucinex
| NDC Code | 63824-273-64 |
| Proprietary Name | Mucinex |
| Package Description | 1 BOTTLE in 1 CARTON (63824-273-64) > 118 mL in 1 BOTTLE |
| Product NDC | 63824-273 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20090408 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reckitt Benckiser, Inc. |
| Substance Name | GUAIFENESIN |
| Strength Number | 100 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
