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Sunmark nite time - 49348-742-36 - (acetaminophen,dextromethorphan HBr, doxylamine succinate)

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Drug Information of Sunmark nite time

Product NDC: 49348-742
Proprietary Name: Sunmark nite time
Non Proprietary Name: acetaminophen,dextromethorphan HBr, doxylamine succinate
Active Ingredient(s): 500; 15; 6.25    mg/15mL; mg/15mL; mg/15mL & nbsp;   acetaminophen,dextromethorphan HBr, doxylamine succinate
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Sunmark nite time

Product NDC: 49348-742
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20060428

Package Information of Sunmark nite time

Package NDC: 49348-742-36
Package Description: 177 mL in 1 BOTTLE (49348-742-36)

NDC Information of Sunmark nite time

NDC Code 49348-742-36
Proprietary Name Sunmark nite time
Package Description 177 mL in 1 BOTTLE (49348-742-36)
Product NDC 49348-742
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen,dextromethorphan HBr, doxylamine succinate
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20060428
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
Strength Number 500; 15; 6.25
Strength Unit mg/15mL; mg/15mL; mg/15mL
Pharmaceutical Classes

Complete Information of Sunmark nite time


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