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Nite Time Cold Multi-Symptom - 55910-555-08 - (Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl)

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Drug Information of Nite Time Cold Multi-Symptom

Product NDC: 55910-555
Proprietary Name: Nite Time Cold Multi-Symptom
Non Proprietary Name: Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl
Active Ingredient(s): 325; 2; 10; 5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Nite Time Cold Multi-Symptom

Product NDC: 55910-555
Labeler Name: DOLGENCORP, LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20050721

Package Information of Nite Time Cold Multi-Symptom

Package NDC: 55910-555-08
Package Description: 1 BLISTER PACK in 1 CARTON (55910-555-08) > 24 CAPSULE in 1 BLISTER PACK

NDC Information of Nite Time Cold Multi-Symptom

NDC Code 55910-555-08
Proprietary Name Nite Time Cold Multi-Symptom
Package Description 1 BLISTER PACK in 1 CARTON (55910-555-08) > 24 CAPSULE in 1 BLISTER PACK
Product NDC 55910-555
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Chlorpheniramine maleate, Dextromethorphan HBr, Phenylephrine HCl
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050721
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name DOLGENCORP, LLC
Substance Name ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 2; 10; 5
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of Nite Time Cold Multi-Symptom


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