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sunmark nite time d - 49348-845-49 - (Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Pseudoephedrine Hydrochloride)

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Drug Information of sunmark nite time d

Product NDC: 49348-845
Proprietary Name: sunmark nite time d
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Pseudoephedrine Hydrochloride
Active Ingredient(s): 500; 15; 6.25; 30    mg/15mL; mg/15mL; mg/15mL; mg/15mL & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Pseudoephedrine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of sunmark nite time d

Product NDC: 49348-845
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20030824

Package Information of sunmark nite time d

Package NDC: 49348-845-49
Package Description: 295 mL in 1 BOTTLE (49348-845-49)

NDC Information of sunmark nite time d

NDC Code 49348-845-49
Proprietary Name sunmark nite time d
Package Description 295 mL in 1 BOTTLE (49348-845-49)
Product NDC 49348-845
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Pseudoephedrine Hydrochloride
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20030824
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PSEUDOEPHEDRINE HYDROCHLORIDE
Strength Number 500; 15; 6.25; 30
Strength Unit mg/15mL; mg/15mL; mg/15mL; mg/15mL
Pharmaceutical Classes

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