PANADOL - 0135-0537-03 - (acetaminophen)

Alphabetical Index


Drug Information of PANADOL

Product NDC: 0135-0537
Proprietary Name: PANADOL
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 PANADOL

Product NDC: 0135-0537
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20121015

Package Information of PANADOL

Package NDC: 0135-0537-03
Package Description: 1 BOTTLE in 1 CARTON (0135-0537-03) > 118 mL in 1 BOTTLE

NDC Information of PANADOL

NDC Code 0135-0537-03
Proprietary Name PANADOL
Package Description 1 BOTTLE in 1 CARTON (0135-0537-03) > 118 mL in 1 BOTTLE
Product NDC 0135-0537
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen
Dosage Form Name LIQUID
Route Name ORAL
Start Marketing Date 20121015
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name ACETAMINOPHEN
Strength Number 160
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of PANADOL


General Information