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Sunmark pain reliever - 49348-042-14 - (Acetaminophen)

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Drug Information of Sunmark pain reliever

Product NDC: 49348-042
Proprietary Name: Sunmark pain reliever
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Sunmark pain reliever

Product NDC: 49348-042
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20030811

Package Information of Sunmark pain reliever

Package NDC: 49348-042-14
Package Description: 500 TABLET in 1 BOTTLE (49348-042-14)

NDC Information of Sunmark pain reliever

NDC Code 49348-042-14
Proprietary Name Sunmark pain reliever
Package Description 500 TABLET in 1 BOTTLE (49348-042-14)
Product NDC 49348-042
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030811
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name McKesson
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Sunmark pain reliever


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