Ibuprofen - 0615-3527-39 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 0615-3527
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 0615-3527
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA071333
Marketing Category: ANDA
Start Marketing Date: 20091216

Package Information of Ibuprofen

Package NDC: 0615-3527-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-3527-39)

NDC Information of Ibuprofen

NDC Code 0615-3527-39
Proprietary Name Ibuprofen
Package Description 30 TABLET in 1 BLISTER PACK (0615-3527-39)
Product NDC 0615-3527
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091216
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information