IBUPROFEN - 55315-122-80 - (IBUPROFEN)

Alphabetical Index


Drug Information of IBUPROFEN

Product NDC: 55315-122
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: 55315-122
Labeler Name: Fred's Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA078682
Marketing Category: ANDA
Start Marketing Date: 20120409

Package Information of IBUPROFEN

Package NDC: 55315-122-80
Package Description: 1 BOTTLE in 1 BOX (55315-122-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE

NDC Information of IBUPROFEN

NDC Code 55315-122-80
Proprietary Name IBUPROFEN
Package Description 1 BOTTLE in 1 BOX (55315-122-80) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product NDC 55315-122
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 Fred's Inc.
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of IBUPROFEN


General Information