Pregabalin Mylan Pharma (pregabalin)
Generic
- Region
- 🇪🇺 EU
- Active substance
- pregabalin
- Company
- Mylan S.A.S.
- Status
- Withdrawn
- Therapeutic area
- Anxiety Disorders; Neuralgia; Epilepsy
- CHMP opinion
- Thu 23 Apr 2015
- EU approval
- Thu 25 Jun 2015
- Designations
- Generic
- Application
- EMEA/H/C/003962
- ATC
- N03AX16
- Official record
- www.ema.europa.eu
Indication
Epilepsy Pregabalin Mylan Pharma is indicated as adjunctive therapy in adults with partial seizures with or without secondary generalisation. Generalised Anxiety Disorder Pregabalin Mylan Pharma is indicated for the treatment of Generalised Anxiety Disorder (GAD) in adults.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Pregabalin Viatris (previously Pregabalin Mylan) Authorised · Viatris Limited
- 🇪🇺 Lyrica Authorised · Viatris EESV
- 🇪🇺 Pregabalin Viatris Pharma (previously Pregabalin Pfizer) Authorised · Viatris Healthcare Limited
- 🇪🇺 Pregabalin Zentiva Authorised · Zentiva k.s.
- 🇪🇺 Pregabalin Sandoz Authorised · Sandoz GmbH
- 🇪🇺 Pregabalin Accord Authorised · Accord Healthcare S.L.U.
- 🇪🇺 Pregabalin Sandoz GmbH Withdrawn · Sandoz GmbH
- 🇪🇺 Pregabalin Zentiva k.s. Withdrawn · Zentiva k.s.
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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.