METI-DERM Drug Patent Profile
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Which patents cover Meti-derm, and when can generic versions of Meti-derm launch?
Meti-derm is a drug marketed by Schering and is included in one NDA.
The generic ingredient in METI-DERM is prednisolone. There is one drug master file entry for this compound. Eleven suppliers are listed for this compound. Additional details are available on the prednisolone profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Meti-derm
A generic version of METI-DERM was approved as prednisolone by ZHEJIANG XIANJU on May 2nd, 2024.
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Questions you can ask:
- What is the 5 year forecast for METI-DERM?
- What are the global sales for METI-DERM?
- What is Average Wholesale Price for METI-DERM?
Summary for METI-DERM
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 1 |
| Raw Ingredient (Bulk) Api Vendors: | 1 |
| Patent Applications: | 7,377 |
| DailyMed Link: | METI-DERM at DailyMed |
US Patents and Regulatory Information for METI-DERM
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Schering | METI-DERM | prednisolone | CREAM;TOPICAL | 010209-002 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
EU/EMA Drug Approvals for METI-DERM
| Company | Drugname | Inn | Product Number / Indication | Status | Generic | Biosimilar | Orphan | Marketing Authorisation | Marketing Refusal |
|---|---|---|---|---|---|---|---|---|---|
| LE VET B.V. | Equisolon | Prednisolone | EMEA/V/C/002382Alleviation of inflammatory and clinical parameters associated with recurrent airway obstruction (RAO) in horses, in combination with environmental control. | Authorised | no | no | no | 2014-03-12 | |
| >Company | >Drugname | >Inn | >Product Number / Indication | >Status | >Generic | >Biosimilar | >Orphan | >Marketing Authorisation | >Marketing Refusal |

