Wal Tussin - 0363-0516-40 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)

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Drug Information of Wal Tussin

Product NDC: 0363-0516
Proprietary Name: Wal Tussin
Non Proprietary Name: Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Active Ingredient(s): 10; 100; 5    mg/5mL; mg/5mL; mg/5mL & nbsp;   Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Wal Tussin

Product NDC: 0363-0516
Labeler Name: Walgreen Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060714

Package Information of Wal Tussin

Package NDC: 0363-0516-40
Package Description: 1 BOTTLE in 1 CARTON (0363-0516-40) > 355 mL in 1 BOTTLE

NDC Information of Wal Tussin

NDC Code 0363-0516-40
Proprietary Name Wal Tussin
Package Description 1 BOTTLE in 1 CARTON (0363-0516-40) > 355 mL in 1 BOTTLE
Product NDC 0363-0516
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20060714
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Walgreen Company
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 10; 100; 5
Strength Unit mg/5mL; mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of Wal Tussin


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