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sunmark allergy multi symptom - 49348-778-04 - (Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl)

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Drug Information of sunmark allergy multi symptom

Product NDC: 49348-778
Proprietary Name: sunmark allergy multi symptom
Non Proprietary Name: Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl
Active Ingredient(s): 325; 2; 5    mg/1; mg/1; mg/1 & nbsp;   Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of sunmark allergy multi symptom

Product NDC: 49348-778
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part341
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20051206

Package Information of sunmark allergy multi symptom

Package NDC: 49348-778-04
Package Description: 2 BLISTER PACK in 1 CARTON (49348-778-04) > 12 TABLET in 1 BLISTER PACK

NDC Information of sunmark allergy multi symptom

NDC Code 49348-778-04
Proprietary Name sunmark allergy multi symptom
Package Description 2 BLISTER PACK in 1 CARTON (49348-778-04) > 12 TABLET in 1 BLISTER PACK
Product NDC 49348-778
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen, Chlorpheniramine maleate, Phenylephrine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051206
Marketing Category Name OTC MONOGRAPH FINAL
Labeler Name McKesson
Substance Name ACETAMINOPHEN; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 325; 2; 5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes

Complete Information of sunmark allergy multi symptom


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