NiteTime - 33992-0621-0 - (Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine Succinate)

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Drug Information of NiteTime

Product NDC: 33992-0621
Proprietary Name: NiteTime
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine Succinate
Active Ingredient(s): 325; 15; 6.25    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine Succinate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of NiteTime

Product NDC: 33992-0621
Labeler Name: Greenbrier International
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20130104

Package Information of NiteTime

Package NDC: 33992-0621-0
Package Description: 1 BLISTER PACK in 1 CARTON (33992-0621-0) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of NiteTime

NDC Code 33992-0621-0
Proprietary Name NiteTime
Package Description 1 BLISTER PACK in 1 CARTON (33992-0621-0) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 33992-0621
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine Succinate
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20130104
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Greenbrier International
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
Strength Number 325; 15; 6.25
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of NiteTime


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