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Tusnel Pediatric - 54859-602-02 - (Guiafenesin, Pseudoephedrine HCl)

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Drug Information of Tusnel Pediatric

Product NDC: 54859-602
Proprietary Name: Tusnel Pediatric
Non Proprietary Name: Guiafenesin, Pseudoephedrine HCl
Active Ingredient(s): 25; 7.5    mg/mL; mg/mL & nbsp;   Guiafenesin, Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Tusnel Pediatric

Product NDC: 54859-602
Labeler Name: Llorens Pharmaceutical International Division
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060101

Package Information of Tusnel Pediatric

Package NDC: 54859-602-02
Package Description: 60 mL in 1 BOTTLE, DROPPER (54859-602-02)

NDC Information of Tusnel Pediatric

NDC Code 54859-602-02
Proprietary Name Tusnel Pediatric
Package Description 60 mL in 1 BOTTLE, DROPPER (54859-602-02)
Product NDC 54859-602
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Guiafenesin, Pseudoephedrine HCl
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20060101
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Llorens Pharmaceutical International Division
Substance Name GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 25; 7.5
Strength Unit mg/mL; mg/mL
Pharmaceutical Classes

Complete Information of Tusnel Pediatric


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