NiteTime - 30142-609-38 - (Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Pseudoephedrine Hydrochloride)

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Drug Information of NiteTime

Product NDC: 30142-609
Proprietary Name: NiteTime
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 NiteTime

Product NDC: 30142-609
Labeler Name: Kroger Company
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 19940509

Package Information of NiteTime

Package NDC: 30142-609-38
Package Description: 295 mL in 1 BOTTLE (30142-609-38)

NDC Information of NiteTime

NDC Code 30142-609-38
Proprietary Name NiteTime
Package Description 295 mL in 1 BOTTLE (30142-609-38)
Product NDC 30142-609
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 19940509
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Kroger Company
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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