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TUSSI PRES PEDIATRIC - 52083-232-01 - (GUAIFENESIN, PHENYLEPHRINE HCL,DEXTROMETHORPHAN HYDROBROMIDE)

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Drug Information of TUSSI PRES PEDIATRIC

Product NDC: 52083-232
Proprietary Name: TUSSI PRES PEDIATRIC
Non Proprietary Name: GUAIFENESIN, PHENYLEPHRINE HCL,DEXTROMETHORPHAN HYDROBROMIDE
Active Ingredient(s): 5; 75; 2.5    mg/5mL; mg/5mL; mg/5mL & nbsp;   GUAIFENESIN, PHENYLEPHRINE HCL,DEXTROMETHORPHAN HYDROBROMIDE
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of TUSSI PRES PEDIATRIC

Product NDC: 52083-232
Labeler Name: KRAMER NOVIS
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20110324

Package Information of TUSSI PRES PEDIATRIC

Package NDC: 52083-232-01
Package Description: 30 mL in 1 BOTTLE (52083-232-01)

NDC Information of TUSSI PRES PEDIATRIC

NDC Code 52083-232-01
Proprietary Name TUSSI PRES PEDIATRIC
Package Description 30 mL in 1 BOTTLE (52083-232-01)
Product NDC 52083-232
Product Type Name HUMAN OTC DRUG
Non Proprietary Name GUAIFENESIN, PHENYLEPHRINE HCL,DEXTROMETHORPHAN HYDROBROMIDE
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 20110324
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name KRAMER NOVIS
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 5; 75; 2.5
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of TUSSI PRES PEDIATRIC


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