Ibuprofen - 68788-9133-3 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 68788-9133
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 68788-9133
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date: 19880524

Package Information of Ibuprofen

Package NDC: 68788-9133-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9133-3)

NDC Information of Ibuprofen

NDC Code 68788-9133-3
Proprietary Name Ibuprofen
Package Description 30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (68788-9133-3)
Product NDC 68788-9133
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19880524
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information