Nighttime - 50804-480-16 - (Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate)

Alphabetical Index


Drug Information of Nighttime

Product NDC: 50804-480
Proprietary Name: Nighttime
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Active Ingredient(s): 325; 15; 6.25    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Nighttime

Product NDC: 50804-480
Labeler Name: Geiss, Destin & Dunn, Inc (Goodsense)
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120701

Package Information of Nighttime

Package NDC: 50804-480-16
Package Description: 2 BLISTER PACK in 1 CARTON (50804-480-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Nighttime

NDC Code 50804-480-16
Proprietary Name Nighttime
Package Description 2 BLISTER PACK in 1 CARTON (50804-480-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 50804-480
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120701
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Geiss, Destin & Dunn, Inc (Goodsense)
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 Nighttime


General Information