IBUPROFEN - 37205-328-57 - (IBUPROFEN)

Alphabetical Index


Drug Information of IBUPROFEN

Product NDC: 37205-328
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: 37205-328
Labeler Name: Cardinal Health
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078682
Marketing Category: ANDA
Start Marketing Date: 20120409

Package Information of IBUPROFEN

Package NDC: 37205-328-57
Package Description: 80 CAPSULE, LIQUID FILLED in 1 BOTTLE (37205-328-57)

NDC Information of IBUPROFEN

NDC Code 37205-328-57
Proprietary Name IBUPROFEN
Package Description 80 CAPSULE, LIQUID FILLED in 1 BOTTLE (37205-328-57)
Product NDC 37205-328
Product Type Name HUMAN OTC DRUG
Non Proprietary Name IBUPROFEN
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120409
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of IBUPROFEN


General Information