Advil - 0573-0133-02 - (ibuprofen sodium)

Alphabetical Index


Drug Information of Advil

Product NDC: 0573-0133
Proprietary Name: Advil
Non Proprietary Name: ibuprofen sodium
Active Ingredient(s): 256    mg/1 & nbsp;   ibuprofen sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Advil

Product NDC: 0573-0133
Labeler Name: Pfizer Consumer Healthcare
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA201803
Marketing Category: NDA
Start Marketing Date: 20130708

Package Information of Advil

Package NDC: 0573-0133-02
Package Description: 50 PACKET in 1 TRAY (0573-0133-02) > 2 TABLET, COATED in 1 PACKET

NDC Information of Advil

NDC Code 0573-0133-02
Proprietary Name Advil
Package Description 50 PACKET in 1 TRAY (0573-0133-02) > 2 TABLET, COATED in 1 PACKET
Product NDC 0573-0133
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ibuprofen sodium
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20130708
Marketing Category Name NDA
Labeler Name Pfizer Consumer Healthcare
Substance Name IBUPROFEN SODIUM
Strength Number 256
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Advil


General Information