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night relief - 55312-977-53 - (Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate)

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Drug Information of night relief

Product NDC: 55312-977
Proprietary Name: night relief
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 night relief

Product NDC: 55312-977
Labeler Name: Western Family Foods Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20070509

Package Information of night relief

Package NDC: 55312-977-53
Package Description: 1 BLISTER PACK in 1 CARTON (55312-977-53) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of night relief

NDC Code 55312-977-53
Proprietary Name night relief
Package Description 1 BLISTER PACK in 1 CARTON (55312-977-53) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 55312-977
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 20070509
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Western Family Foods Inc
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 night relief


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