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SUNMARK TUSSIN CF - 49348-737-37 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)

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Drug Information of SUNMARK TUSSIN CF

Product NDC: 49348-737
Proprietary Name: SUNMARK 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 SUNMARK TUSSIN CF

Product NDC: 49348-737
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060502

Package Information of SUNMARK TUSSIN CF

Package NDC: 49348-737-37
Package Description: 1 BOTTLE in 1 CARTON (49348-737-37) > 236 mL in 1 BOTTLE

NDC Information of SUNMARK TUSSIN CF

NDC Code 49348-737-37
Proprietary Name SUNMARK TUSSIN CF
Package Description 1 BOTTLE in 1 CARTON (49348-737-37) > 236 mL in 1 BOTTLE
Product NDC 49348-737
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20060502
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
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 SUNMARK TUSSIN CF


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