Composition
- Active ingredients
- IBUPROFEN 600MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- IBUPROFEN 200MG · TabletANDA202312-001 · Over the counter
- IBUPROFEN 200MG · TabletANDA206989-001 · Discontinued
- IBUPROFEN 200MG · TabletANDA207052-001 · Discontinued
- IBUPROFEN 100MG/5ML · SuspensionANDA210149-001 · Over the counter
- IBUPROFEN 600MG · TabletANDA070437-001 · Discontinued
- IBUPROFEN 200MG · TabletANDA070493-001 · Discontinued
- IBUPROFEN 600MG · TabletANDA070709-001 · Discontinued
- IBUPROFEN 200MG · TabletANDA071163-001 · Discontinued
- IBUPROFEN 200MG · TabletANDA071229-001 · Discontinued
- IBUPROFEN 300MG · TabletANDA071230-001 · Discontinued
- IBUPROFEN 200MG · TabletANDA071765-001 · Discontinued
- IBUPROFEN 200MG · TabletANDA071870-001 · Discontinued
- IBUPROFEN 800MG · TabletANDA071938-001 · Discontinued
- IBUPROFEN 400MG · TabletANDA072064-001 · Discontinued
- IBUPROFEN 200MG · TabletANDA072249-001 · Discontinued
- IBUPROFEN 200MG · TabletANDA072903-001 · Discontinued
- IBUPROFEN 200MG · TabletANDA075139-001 · Over the counter
- IBUPROFEN 200MG · TabletANDA091237-001 · Over the counter
- IBUPROFEN 100MG/5ML · SuspensionANDA200457-001 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA071125.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Ibuprofen
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Purepac Pharm
- Status
- Discontinued
- Application
- ANDA071125-001