Composition
- Active ingredients
- IBUPROFEN 800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- IBUPROFEN 100MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · SuspensionNDA019842-001 · Discontinued
- IBUPROFEN 100MG · Tablet, chewableNDA020135-002 · Discontinued
- IBUPROFEN 50MG · Tablet, chewableNDA020135-001 · Discontinued
- IBUPROFEN 600MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA017463-004 · Discontinued
- IBUPROFEN 400MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA017463-002 · Discontinued
- IBUPROFEN 800MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletThis page
- IBUPROFEN 300MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · TabletNDA017463-003 · Discontinued
- IBUPROFEN 100MG · TabletNDA020418-001 · Discontinued
- IBUPROFEN 40MG/ML · Suspension/dropsNDA020476-001 · Discontinued
At a glance
- Brand name
- Motrin
- Active substance
- ibuprofen
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Mcneil Consumer
- Status
- Discontinued
- FDA approval
- 19 Sept 1974
- Application
- NDA017463-005