ADVIL - 0573-0169-17 - (IBUPROFEN)

Alphabetical Index


Drug Information of ADVIL

Product NDC: 0573-0169
Proprietary Name: ADVIL
Non Proprietary Name: IBUPROFEN
Active Ingredient(s): 200    mg/1 & nbsp;   IBUPROFEN
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of ADVIL

Product NDC: 0573-0169
Labeler Name: Pfizer Consumer Healthcare
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA020402
Marketing Category: NDA
Start Marketing Date: 19950410

Package Information of ADVIL

Package NDC: 0573-0169-17
Package Description: 3000 POUCH in 1 CASE (0573-0169-17) > 2 CAPSULE, LIQUID FILLED in 1 POUCH

NDC Information of ADVIL

NDC Code 0573-0169-17
Proprietary Name ADVIL
Package Description 3000 POUCH in 1 CASE (0573-0169-17) > 2 CAPSULE, LIQUID FILLED in 1 POUCH
Product NDC 0573-0169
Product Type Name HUMAN OTC DRUG
Non Proprietary Name IBUPROFEN
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 19950410
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