Motrin - 50580-109-29 - (Ibuprofen)

Alphabetical Index


Drug Information of Motrin

Product NDC: 50580-109
Proprietary Name: Motrin
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 Motrin

Product NDC: 50580-109
Labeler Name: McNeil Consumer Healthcare Div McNeil-PPC, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA019012
Marketing Category: NDA
Start Marketing Date: 20050201

Package Information of Motrin

Package NDC: 50580-109-29
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (50580-109-29) > 125 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

NDC Information of Motrin

NDC Code 50580-109-29
Proprietary Name Motrin
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (50580-109-29) > 125 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product NDC 50580-109
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ibuprofen
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050201
Marketing Category Name NDA
Labeler Name McNeil Consumer Healthcare Div McNeil-PPC, Inc
Substance Name IBUPROFEN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Motrin


General Information