Delsym - 63824-215-66 - (acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride)

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Drug Information of Delsym

Product NDC: 63824-215
Proprietary Name: Delsym
Non Proprietary Name: acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Active Ingredient(s): 650; 20; 400; 10    mg/20mL; mg/20mL; mg/20mL; mg/20mL & nbsp;   acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Delsym

Product NDC: 63824-215
Labeler Name: Reckitt Benckiser LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130331

Package Information of Delsym

Package NDC: 63824-215-66
Package Description: 180 mL in 1 BOTTLE (63824-215-66)

NDC Information of Delsym

NDC Code 63824-215-66
Proprietary Name Delsym
Package Description 180 mL in 1 BOTTLE (63824-215-66)
Product NDC 63824-215
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20130331
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Reckitt Benckiser LLC
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 650; 20; 400; 10
Strength Unit mg/20mL; mg/20mL; mg/20mL; mg/20mL
Pharmaceutical Classes

Complete Information of Delsym


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