MYTREX Drug Patent Profile
✉ Email this page to a colleague
When do Mytrex patents expire, and when can generic versions of Mytrex launch?
Mytrex is a drug marketed by Savage Labs and is included in four NDAs.
The generic ingredient in MYTREX is nystatin; triamcinolone acetonide. There are eight drug master file entries for this compound. Eighteen suppliers are listed for this compound. Additional details are available on the nystatin; triamcinolone acetonide profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Mytrex
A generic version of MYTREX was approved as nystatin; triamcinolone acetonide by FOUGERA PHARMS INC on October 8th, 1985.
AI Deep Research
Questions you can ask:
- What is the 5 year forecast for MYTREX?
- What are the global sales for MYTREX?
- What is Average Wholesale Price for MYTREX?
Summary for MYTREX
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 4 |
| DailyMed Link: | MYTREX at DailyMed |
US Patents and Regulatory Information for MYTREX
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Savage Labs | MYTREX A | neomycin sulfate; triamcinolone acetonide | CREAM;TOPICAL | 062598-001 | Jul 21, 1986 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Savage Labs | MYTREX F | nystatin; triamcinolone acetonide | OINTMENT;TOPICAL | 062601-001 | Oct 9, 1985 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Savage Labs | MYTREX A | neomycin sulfate; triamcinolone acetonide | OINTMENT;TOPICAL | 062609-001 | May 23, 1986 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Savage Labs | MYTREX F | nystatin; triamcinolone acetonide | CREAM;TOPICAL | 062597-001 | Oct 8, 1985 | 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 |
