IBUPROFEN - 50332-0118-4 - (ibuprofen)

Alphabetical Index


Drug Information of IBUPROFEN

Product NDC: 50332-0118
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: 50332-0118
Labeler Name: HART Health
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19870603

Package Information of IBUPROFEN

Package NDC: 50332-0118-4
Package Description: 50 PACKET in 1 BOX, UNIT-DOSE (50332-0118-4) > 2 TABLET in 1 PACKET

NDC Information of IBUPROFEN

NDC Code 50332-0118-4
Proprietary Name IBUPROFEN
Package Description 50 PACKET in 1 BOX, UNIT-DOSE (50332-0118-4) > 2 TABLET in 1 PACKET
Product NDC 50332-0118
Product Type Name HUMAN OTC DRUG
Non Proprietary Name ibuprofen
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19870603
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name HART Health
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of IBUPROFEN


General Information