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sunmark tussin dm - 49348-861-34 - (Dextromethorphan HBr, Guaifenesin)

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Drug Information of sunmark tussin dm

Product NDC: 49348-861
Proprietary Name: sunmark tussin dm
Non Proprietary Name: Dextromethorphan HBr, Guaifenesin
Active Ingredient(s): 10; 100    mg/5mL; mg/5mL & nbsp;   Dextromethorphan HBr, Guaifenesin
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of sunmark tussin dm

Product NDC: 49348-861
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20030624

Package Information of sunmark tussin dm

Package NDC: 49348-861-34
Package Description: 1 BOTTLE in 1 CARTON (49348-861-34) > 118 mL in 1 BOTTLE

NDC Information of sunmark tussin dm

NDC Code 49348-861-34
Proprietary Name sunmark tussin dm
Package Description 1 BOTTLE in 1 CARTON (49348-861-34) > 118 mL in 1 BOTTLE
Product NDC 49348-861
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Dextromethorphan HBr, Guaifenesin
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20030624
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
Strength Number 10; 100
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes

Complete Information of sunmark tussin dm


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