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Mucinex Fast-Max
Mucinex Fast-Max - 63824-193-20 - (Guaifenesin, Phenylephrine Hydrochloride, and Dextromethorphan hydrobromide)
Drug Information of Mucinex Fast-Max
| Product NDC: | 63824-193 |
| Proprietary Name: | Mucinex Fast-Max |
| Non Proprietary Name: | Guaifenesin, Phenylephrine Hydrochloride, and Dextromethorphan hydrobromide |
| Active Ingredient(s): | 10; 200; 5 mg/1; mg/1; mg/1 & nbsp; Guaifenesin, Phenylephrine Hydrochloride, and Dextromethorphan hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Mucinex Fast-Max
| Product NDC: | 63824-193 |
| Labeler Name: | Reckitt Benckiser LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130315 |
Package Information of Mucinex Fast-Max
| Package NDC: | 63824-193-20 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (63824-193-20) > 10 TABLET, COATED in 1 BLISTER PACK |
NDC Information of Mucinex Fast-Max
| NDC Code | 63824-193-20 |
| Proprietary Name | Mucinex Fast-Max |
| Package Description | 2 BLISTER PACK in 1 CARTON (63824-193-20) > 10 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 63824-193 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Guaifenesin, Phenylephrine Hydrochloride, and Dextromethorphan hydrobromide |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20130315 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Reckitt Benckiser LLC |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10; 200; 5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
