Nitetime D - 41250-550-38 - (Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Pseudoephedrine HCl)

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Drug Information of Nitetime D

Product NDC: 41250-550
Proprietary Name: Nitetime D
Non Proprietary Name: Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Pseudoephedrine HCl
Active Ingredient(s): 500; 15; 6.25; 30    mg/15mL; mg/15mL; mg/15mL; mg/15mL & nbsp;   Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Pseudoephedrine HCl
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Nitetime D

Product NDC: 41250-550
Labeler Name: Meijer Distribution Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19940329

Package Information of Nitetime D

Package NDC: 41250-550-38
Package Description: 296 mL in 1 BOTTLE (41250-550-38)

NDC Information of Nitetime D

NDC Code 41250-550-38
Proprietary Name Nitetime D
Package Description 296 mL in 1 BOTTLE (41250-550-38)
Product NDC 41250-550
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Pseudoephedrine HCl
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 19940329
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Meijer Distribution Inc
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

Complete Information of Nitetime D


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