Ibuprofen - 52605-114-10 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 52605-114
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: 52605-114
Labeler Name: Polygen Pharmaceuticals LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091239
Marketing Category: ANDA
Start Marketing Date: 20120605

Package Information of Ibuprofen

Package NDC: 52605-114-10
Package Description: 1000 TABLET, COATED in 1 BOTTLE (52605-114-10)

NDC Information of Ibuprofen

NDC Code 52605-114-10
Proprietary Name Ibuprofen
Package Description 1000 TABLET, COATED in 1 BOTTLE (52605-114-10)
Product NDC 52605-114
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20120605
Marketing Category Name ANDA
Labeler Name Polygen Pharmaceuticals LLC
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information