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Cold Multi-Symptom Daytime Nighttime - 57344-150-02 - (Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride)

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Drug Information of Cold Multi-Symptom Daytime Nighttime

Product NDC: 57344-150
Proprietary Name: Cold Multi-Symptom Daytime Nighttime
Non Proprietary Name: Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Active Ingredient(s):    & nbsp;   Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Cold Multi-Symptom Daytime Nighttime

Product NDC: 57344-150
Labeler Name: AAA Pharmaceutical, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20121228

Package Information of Cold Multi-Symptom Daytime Nighttime

Package NDC: 57344-150-02
Package Description: 1 KIT in 1 CARTON (57344-150-02) * 12 TABLET, COATED in 1 BLISTER PACK * 8 TABLET, COATED in 1 BLISTER PACK

NDC Information of Cold Multi-Symptom Daytime Nighttime

NDC Code 57344-150-02
Proprietary Name Cold Multi-Symptom Daytime Nighttime
Package Description 1 KIT in 1 CARTON (57344-150-02) * 12 TABLET, COATED in 1 BLISTER PACK * 8 TABLET, COATED in 1 BLISTER PACK
Product NDC 57344-150
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Chlorpheniramine Maleate, Dextromethorphan Hydrobromide, and Phenylephrine Hydrochloride
Dosage Form Name KIT
Route Name
Start Marketing Date 20121228
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name AAA Pharmaceutical, Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Cold Multi-Symptom Daytime Nighttime


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