Ibuprofen - 41163-198-80 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 41163-198
Proprietary Name: Ibuprofen
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 Ibuprofen

Product NDC: 41163-198
Labeler Name: EQUALINE (SuperValu)
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078682
Marketing Category: ANDA
Start Marketing Date: 20120110

Package Information of Ibuprofen

Package NDC: 41163-198-80
Package Description: 1 BOTTLE, PLASTIC in 1 BOX (41163-198-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

NDC Information of Ibuprofen

NDC Code 41163-198-80
Proprietary Name Ibuprofen
Package Description 1 BOTTLE, PLASTIC in 1 BOX (41163-198-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
Product NDC 41163-198
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120110
Marketing Category Name ANDA
Labeler Name EQUALINE (SuperValu)
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information