Product NDC: | 50580-110 |
Proprietary Name: | Motrin IB |
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) |
Product NDC: | 50580-110 |
Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA019012 |
Marketing Category: | NDA |
Start Marketing Date: | 20000801 |
Package NDC: | 50580-110-75 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (50580-110-75) > 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
NDC Code | 50580-110-75 |
Proprietary Name | Motrin IB |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (50580-110-75) > 150 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
Product NDC | 50580-110 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ibuprofen |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20000801 |
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 |