Ibuprofen - 11383-151-50 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 11383-151
Proprietary Name: Ibuprofen
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 Ibuprofen

Product NDC: 11383-151
Labeler Name: Weeks & Leo Co., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091239
Marketing Category: ANDA
Start Marketing Date: 20130517

Package Information of Ibuprofen

Package NDC: 11383-151-50
Package Description: 1 BOTTLE in 1 CARTON (11383-151-50) > 50 TABLET, COATED in 1 BOTTLE

NDC Information of Ibuprofen

NDC Code 11383-151-50
Proprietary Name Ibuprofen
Package Description 1 BOTTLE in 1 CARTON (11383-151-50) > 50 TABLET, COATED in 1 BOTTLE
Product NDC 11383-151
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20130517
Marketing Category Name ANDA
Labeler Name Weeks & Leo Co., Inc.
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information