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Multi symptom Nighttime - 68016-202-24 - (Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate)

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Drug Information of Multi symptom Nighttime

Product NDC: 68016-202
Proprietary Name: Multi symptom 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 Multi symptom Nighttime

Product NDC: 68016-202
Labeler Name: Premier Value (Chain Drug Consortium, LLC)
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121115

Package Information of Multi symptom Nighttime

Package NDC: 68016-202-24
Package Description: 2 BLISTER PACK in 1 CARTON (68016-202-24) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Multi symptom Nighttime

NDC Code 68016-202-24
Proprietary Name Multi symptom Nighttime
Package Description 2 BLISTER PACK in 1 CARTON (68016-202-24) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 68016-202
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 20121115
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name Premier Value (Chain Drug Consortium, LLC)
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 Multi symptom Nighttime


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