IBUPROFEN - 25000-133-18 - (ibuprofen)

Alphabetical Index


Drug Information of IBUPROFEN

Product NDC: 25000-133
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: 25000-133
Labeler Name: Marksans Pharma Limited
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA079205
Marketing Category: ANDA
Start Marketing Date: 20110509

Package Information of IBUPROFEN

Package NDC: 25000-133-18
Package Description: 4 BAG in 1 BOX (25000-133-18) > 2500 CAPSULE, LIQUID FILLED in 1 BAG

NDC Information of IBUPROFEN

NDC Code 25000-133-18
Proprietary Name IBUPROFEN
Package Description 4 BAG in 1 BOX (25000-133-18) > 2500 CAPSULE, LIQUID FILLED in 1 BAG
Product NDC 25000-133
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ibuprofen
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20110509
Marketing Category Name ANDA
Labeler Name Marksans Pharma Limited
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of IBUPROFEN


General Information