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Sunmark Pain Reliever - 49348-268-27 - (Acetaminophen)

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Drug Information of Sunmark Pain Reliever

Product NDC: 49348-268
Proprietary Name: Sunmark Pain Reliever
Non Proprietary Name: Acetaminophen
Active Ingredient(s): 80    mg/.8mL & nbsp;   Acetaminophen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Sunmark Pain Reliever

Product NDC: 49348-268
Labeler Name: McKesson
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20030919

Package Information of Sunmark Pain Reliever

Package NDC: 49348-268-27
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (49348-268-27) > 30 mL in 1 BOTTLE, DROPPER

NDC Information of Sunmark Pain Reliever

NDC Code 49348-268-27
Proprietary Name Sunmark Pain Reliever
Package Description 1 BOTTLE, DROPPER in 1 CARTON (49348-268-27) > 30 mL in 1 BOTTLE, DROPPER
Product NDC 49348-268
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Acetaminophen
Dosage Form Name SUSPENSION/ DROPS
Route Name ORAL
Start Marketing Date 20030919
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name McKesson
Substance Name ACETAMINOPHEN
Strength Number 80
Strength Unit mg/.8mL
Pharmaceutical Classes

Complete Information of Sunmark Pain Reliever


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