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Mucinex Fast-Max - 63824-014-66 - (dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride)

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Drug Information of Mucinex Fast-Max

Product NDC: 63824-014
Proprietary Name: Mucinex Fast-Max
Non Proprietary Name: dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Active Ingredient(s): 20; 400; 10    mg/20mL; mg/20mL; mg/20mL & nbsp;   dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Mucinex Fast-Max

Product NDC: 63824-014
Labeler Name: Reckitt Benckiser LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120207

Package Information of Mucinex Fast-Max

Package NDC: 63824-014-66
Package Description: 180 mL in 1 BOTTLE (63824-014-66)

NDC Information of Mucinex Fast-Max

NDC Code 63824-014-66
Proprietary Name Mucinex Fast-Max
Package Description 180 mL in 1 BOTTLE (63824-014-66)
Product NDC 63824-014
Product Type Name HUMAN OTC DRUG
Non Proprietary Name dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20120207
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Reckitt Benckiser LLC
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 20; 400; 10
Strength Unit mg/20mL; mg/20mL; mg/20mL
Pharmaceutical Classes

Complete Information of Mucinex Fast-Max


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