Ibuprofen - 17856-5309-5 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 17856-5309
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 100    mg/5mL & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 17856-5309
Labeler Name: Atlantic Biologicals Corps
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA074937
Marketing Category: ANDA
Start Marketing Date: 19990207

Package Information of Ibuprofen

Package NDC: 17856-5309-5
Package Description: 5 mL in 1 CUP (17856-5309-5)

NDC Information of Ibuprofen

NDC Code 17856-5309-5
Proprietary Name Ibuprofen
Package Description 5 mL in 1 CUP (17856-5309-5)
Product NDC 17856-5309
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 19990207
Marketing Category Name ANDA
Labeler Name Atlantic Biologicals Corps
Substance Name IBUPROFEN
Strength Number 100
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information