PANADOL - 0135-0136-04 - (acetaminophen)

Alphabetical Index


Drug Information of PANADOL

Product NDC: 0135-0136
Proprietary Name: PANADOL
Non Proprietary Name: acetaminophen
Active Ingredient(s): 500    mg/1 & nbsp;   acetaminophen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of PANADOL

Product NDC: 0135-0136
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: 0135-0136-04
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0135-0136-04)

NDC Information of PANADOL

NDC Code 0135-0136-04
Proprietary Name PANADOL
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0135-0136-04)
Product NDC 0135-0136
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen
Dosage Form Name TABLET, FILM COATED
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