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Guaifenesin Phenylephrine Dextromethorphan - 52083-249-60 - (Guaifenesin, phenylephrine HCL, Dextromethorphan)

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Drug Information of Guaifenesin Phenylephrine Dextromethorphan

Product NDC: 52083-249
Proprietary Name: Guaifenesin Phenylephrine Dextromethorphan
Non Proprietary Name: Guaifenesin, phenylephrine HCL, Dextromethorphan
Active Ingredient(s): 20; 400; 10    mg/1; mg/1; mg/1 & nbsp;   Guaifenesin, phenylephrine HCL, Dextromethorphan
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Guaifenesin Phenylephrine Dextromethorphan

Product NDC: 52083-249
Labeler Name: Kramer Novis.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120718

Package Information of Guaifenesin Phenylephrine Dextromethorphan

Package NDC: 52083-249-60
Package Description: 60 TABLET, COATED in 1 BOTTLE (52083-249-60)

NDC Information of Guaifenesin Phenylephrine Dextromethorphan

NDC Code 52083-249-60
Proprietary Name Guaifenesin Phenylephrine Dextromethorphan
Package Description 60 TABLET, COATED in 1 BOTTLE (52083-249-60)
Product NDC 52083-249
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guaifenesin, phenylephrine HCL, Dextromethorphan
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20120718
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kramer Novis.
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 20; 400; 10
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Guaifenesin Phenylephrine Dextromethorphan


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