FDA
Diclofenac Potassium
The FDA lists this product in 21 strengths and forms.
Composition
- Active ingredients
- DICLOFENAC POTASSIUM 50MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- DICLOFENAC POTASSIUM 50MG · TabletANDA215585-001 · Prescription
- DICLOFENAC POTASSIUM 25MG · TabletANDA215750-002 · Prescription
- DICLOFENAC POTASSIUM 50MG · TabletANDA215750-001 · Prescription
- DICLOFENAC POTASSIUM 25MG · CapsuleANDA204648-001 · Prescription
- DICLOFENAC POTASSIUM 50MG · For solutionANDA217010-001 · Prescription
- DICLOFENAC POTASSIUM 50MG · For solutionANDA218011-001 · Prescription
- DICLOFENAC POTASSIUM 50MG · TabletANDA075463-001 · Prescription
- DICLOFENAC POTASSIUM 50MG · TabletANDA075582-001 · Discontinued
- DICLOFENAC POTASSIUM 50MG · For solutionANDA215891-001 · Prescription
- DICLOFENAC POTASSIUM 50MG · For solutionANDA202964-001 · Prescription
- DICLOFENAC POTASSIUM 50MG · TabletANDA075152-001 · Discontinued
- DICLOFENAC POTASSIUM 50MG · Tablet
At a glance
- Brand name
- Diclofenac Potassium
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Sun Pharm Industries
- Status
- Discontinued
- FDA approval
- 21 Feb 2002
- Application
- ANDA075470-001