ADVIL - 0573-0161-85 - (ibuprofen)

Alphabetical Index


Drug Information of ADVIL

Product NDC: 0573-0161
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: 0573-0161
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: 0573-0161-85
Package Description: 1 BOTTLE in 1 CARTON (0573-0161-85) > 225 TABLET, COATED in 1 BOTTLE

NDC Information of ADVIL

NDC Code 0573-0161-85
Proprietary Name ADVIL
Package Description 1 BOTTLE in 1 CARTON (0573-0161-85) > 225 TABLET, COATED in 1 BOTTLE
Product NDC 0573-0161
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