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Mucinex Fast-Max - 63824-190-30 - (Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride)

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Drug Information of Mucinex Fast-Max

Product NDC: 63824-190
Proprietary Name: Mucinex Fast-Max
Non Proprietary Name: Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride
Active Ingredient(s): 325; 200; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Mucinex Fast-Max

Product NDC: 63824-190
Labeler Name: Reckitt Benckiser LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120627

Package Information of Mucinex Fast-Max

Package NDC: 63824-190-30
Package Description: 3 BLISTER PACK in 1 CARTON (63824-190-30) > 10 TABLET, COATED in 1 BLISTER PACK

NDC Information of Mucinex Fast-Max

NDC Code 63824-190-30
Proprietary Name Mucinex Fast-Max
Package Description 3 BLISTER PACK in 1 CARTON (63824-190-30) > 10 TABLET, COATED in 1 BLISTER PACK
Product NDC 63824-190
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Guaifenesin, and Phenylephrine Hydrochloride
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20120627
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Reckitt Benckiser LLC
Substance Name ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 200; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Mucinex Fast-Max


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