Panadol - 0135-0459-02 - (acetaminophen and phenylephrine HCl)

Alphabetical Index


Drug Information of Panadol

Product NDC: 0135-0459
Proprietary Name: Panadol
Non Proprietary Name: acetaminophen and phenylephrine HCl
Active Ingredient(s): 500; 5    mg/1; mg/1 & nbsp;   acetaminophen and phenylephrine HCl
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Panadol

Product NDC: 0135-0459
Labeler Name: GlaxoSmithKline Consumer Healthcare LP
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 20110831

Package Information of Panadol

Package NDC: 0135-0459-02
Package Description: 3 BLISTER PACK in 1 CARTON (0135-0459-02) > 8 TABLET in 1 BLISTER PACK

NDC Information of Panadol

NDC Code 0135-0459-02
Proprietary Name Panadol
Package Description 3 BLISTER PACK in 1 CARTON (0135-0459-02) > 8 TABLET in 1 BLISTER PACK
Product NDC 0135-0459
Product Type Name HUMAN OTC DRUG
Non Proprietary Name acetaminophen and phenylephrine HCl
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110831
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name GlaxoSmithKline Consumer Healthcare LP
Substance Name ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
Strength Number 500; 5
Strength Unit mg/1; mg/1
Pharmaceutical Classes

Complete Information of Panadol


General Information