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Night Time Original - 59640-112-01 - (Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate,)

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Drug Information of Night Time Original

Product NDC: 59640-112
Proprietary Name: Night Time Original
Non Proprietary Name: Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate,
Active Ingredient(s): 500; 15; 6.25    mg/15mL; mg/15mL; mg/15mL & nbsp;   Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate,
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of Night Time Original

Product NDC: 59640-112
Labeler Name: H.E.B
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20090616

Package Information of Night Time Original

Package NDC: 59640-112-01
Package Description: 296 mL in 1 BOTTLE, PLASTIC (59640-112-01)

NDC Information of Night Time Original

NDC Code 59640-112-01
Proprietary Name Night Time Original
Package Description 296 mL in 1 BOTTLE, PLASTIC (59640-112-01)
Product NDC 59640-112
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate,
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20090616
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name H.E.B
Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
Strength Number 500; 15; 6.25
Strength Unit mg/15mL; mg/15mL; mg/15mL
Pharmaceutical Classes

Complete Information of Night Time Original


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