Ibuprofen - 70253-292-08 - (Ibuprofen)

Alphabetical Index


Drug Information of Ibuprofen

Product NDC: 70253-292
Proprietary Name: Ibuprofen
Non Proprietary Name: Ibuprofen
Active Ingredient(s): 200    mg/1 & nbsp;   Ibuprofen
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ibuprofen

Product NDC: 70253-292
Labeler Name: NASH-FINCH COMPANY
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: 70253-292-08
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (70253-292-08) > 24 CAPSULE, COATED in 1 BOTTLE, PLASTIC

NDC Information of Ibuprofen

NDC Code 70253-292-08
Proprietary Name Ibuprofen
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (70253-292-08) > 24 CAPSULE, COATED in 1 BOTTLE, PLASTIC
Product NDC 70253-292
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name CAPSULE, COATED
Route Name ORAL
Start Marketing Date 19880524
Marketing Category Name OTC MONOGRAPH NOT FINAL
Labeler Name NASH-FINCH COMPANY
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ibuprofen


General Information