ADVIL - 0573-0151-14 - (ibuprofen)

Alphabetical Index


Drug Information of ADVIL

Product NDC: 0573-0151
Proprietary Name: ADVIL
Non Proprietary Name: ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ADVIL

Product NDC: 0573-0151
Labeler Name: Pfizer Consumer Healthcare
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA018989
Marketing Category: NDA
Start Marketing Date: 19840518

Package Information of ADVIL

Package NDC: 0573-0151-14
Package Description: 1 VIAL in 1 BLISTER PACK (0573-0151-14) > 10 TABLET, COATED in 1 VIAL

NDC Information of ADVIL

NDC Code 0573-0151-14
Proprietary Name ADVIL
Package Description 1 VIAL in 1 BLISTER PACK (0573-0151-14) > 10 TABLET, COATED in 1 VIAL
Product NDC 0573-0151
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 19840518
Marketing Category Name NDA
Labeler Name Pfizer Consumer Healthcare
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of ADVIL


General Information