Advil - 66715-9700-8 - (Ibuprofen)

Alphabetical Index


Drug Information of Advil

Product NDC: 66715-9700
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: 66715-9700
Labeler Name: Lil' Drug Store Products, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA018989
Marketing Category: NDA
Start Marketing Date: 20100222

Package Information of Advil

Package NDC: 66715-9700-8
Package Description: 6 POUCH in 1 CARTON (66715-9700-8) > 2 TABLET, COATED in 1 POUCH

NDC Information of Advil

NDC Code 66715-9700-8
Proprietary Name Advil
Package Description 6 POUCH in 1 CARTON (66715-9700-8) > 2 TABLET, COATED in 1 POUCH
Product NDC 66715-9700
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20100222
Marketing Category Name NDA
Labeler Name Lil' Drug Store Products, Inc.
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Advil


General Information