Zoledronic acid Teva (zoledronic acid)
Generic
- Region
- 🇪🇺 EU
- Active substance
- zoledronic acid
- Company
- Teva B.V.
- Status
- Authorised
- Therapeutic area
- Fractures, Bone; Cancer
- CHMP opinion
- Thu 15 Mar 2012
- EU approval
- Thu 16 Aug 2012
- Designations
- Generic
- Application
- EMEA/H/C/002439
- ATC
- M05BA08
- Official record
- www.ema.europa.eu
Indication
Prevention of skeletal-related events and treatment of tumour-induced hypercalcaemia.
Regulatory milestones
No milestones recorded in the last year.
Same substance in other markets
- 🇪🇺 Zoledronic acid Mylan Authorised · Mylan Pharmaceuticals Limited
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- 🇪🇺 Zoledronic Acid Hospira Withdrawn · Pfizer Europe MA EEIG
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- 🇪🇺 Zoledronic Acid Accord Authorised · Accord Healthcare S.L.U.
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- 🇪🇺 Zoledronic acid Teva Pharma Withdrawn · Teva B.V.
- 🇪🇺 Zoledronic acid Teva Generics Withdrawn · Teva Generics B.V
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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.