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sunmark pain reliever - 49348-309-30 - (Acetaminophen)

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Drug Information of sunmark pain reliever

Product NDC: 49348-309
Proprietary Name: sunmark pain reliever
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 160    mg/5mL & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Coding System: National Drug Codes(NDC)

Labeler Information of sunmark pain reliever

Product NDC: 49348-309
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110926

Package Information of sunmark pain reliever

Package NDC: 49348-309-30
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (49348-309-30) > 60 mL in 1 BOTTLE, DROPPER

NDC Information of sunmark pain reliever

NDC Code 49348-309-30
Proprietary Name sunmark pain reliever
Package Description 1 BOTTLE, DROPPER in 1 CARTON (49348-309-30) > 60 mL in 1 BOTTLE, DROPPER
Product NDC 49348-309
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20110926
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name McKesson
Substance Name ACETAMINOPHEN
Strength Number 160
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of sunmark pain reliever


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