PANADOL - 0135-0135-03 - (acetaminophen)

Alphabetical Index


Drug Information of PANADOL

Product NDC: 0135-0135
Proprietary Name: PANADOL
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 PANADOL

Product NDC: 0135-0135
Labeler Name: GlaxoSmithKline Consumer Healtcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110318

Package Information of PANADOL

Package NDC: 0135-0135-03
Package Description: 60 TABLET in 1 BOTTLE (0135-0135-03)

NDC Information of PANADOL

NDC Code 0135-0135-03
Proprietary Name PANADOL
Package Description 60 TABLET in 1 BOTTLE (0135-0135-03)
Product NDC 0135-0135
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110318
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name GlaxoSmithKline Consumer Healtcare LP
Substance Name ACETAMINOPHEN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of PANADOL


General Information