MOMETASONE Drug Patent Profile
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When do Mometasone patents expire, and when can generic versions of Mometasone launch?
Mometasone is a drug marketed by Chartwell Molecular, Cosette Pharms Nc, Fougera Pharms, Glenmark Pharms, Sun Pharma Canada, Cosette, Encube, Glenmark Pharms Ltd, Padagis Israel, Padagis Us, Torrent, Amneal, Amneal Pharms, Apotex, Aurobindo Pharma, and Naspress. and is included in twenty-five NDAs.
The generic ingredient in MOMETASONE is mometasone furoate. There are thirty drug master file entries for this compound. Twenty-seven suppliers are listed for this compound. Additional details are available on the mometasone furoate profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Mometasone
A generic version of MOMETASONE was approved as mometasone furoate by PADAGIS US on March 18th, 2002.
AI Deep Research
Questions you can ask:
- What is the 5 year forecast for MOMETASONE?
- What are the global sales for MOMETASONE?
- What is Average Wholesale Price for MOMETASONE?
Summary for MOMETASONE
| US Patents: | 0 |
| Applicants: | 16 |
| NDAs: | 25 |
| Drug Prices: | Drug price information for MOMETASONE |
| Drug Sales Revenues: | Drug sales revenues for MOMETASONE |
| DailyMed Link: | MOMETASONE at DailyMed |
US Patents and Regulatory Information for MOMETASONE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Chartwell Molecular | MOMETASONE FUROATE | mometasone furoate | CREAM;TOPICAL | 076591-001 | Apr 18, 2007 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Torrent | MOMETASONE FUROATE | mometasone furoate | OINTMENT;TOPICAL | 207899-001 | Jul 13, 2018 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Aurobindo Pharma | MOMETASONE FUROATE | mometasone furoate | SPRAY, METERED;NASAL | 217498-001 | Nov 22, 2024 | 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 |



