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wal tussin cf - 0363-0704-26 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)

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Drug Information of wal tussin cf

Product NDC: 0363-0704
Proprietary Name: wal tussin cf
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 cf

Product NDC: 0363-0704
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 cf

Package NDC: 0363-0704-26
Package Description: 1 BOTTLE in 1 CARTON (0363-0704-26) > 118 mL in 1 BOTTLE

NDC Information of wal tussin cf

NDC Code 0363-0704-26
Proprietary Name wal tussin cf
Package Description 1 BOTTLE in 1 CARTON (0363-0704-26) > 118 mL in 1 BOTTLE
Product NDC 0363-0704
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 cf


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