A-METHAPRED Drug Patent Profile
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When do A-methapred patents expire, and when can generic versions of A-methapred launch?
A-methapred is a drug marketed by Abbott, Hospira, and Hospira Inc. and is included in fourteen NDAs.
The generic ingredient in A-METHAPRED is methylprednisolone sodium succinate. There are forty drug master file entries for this compound. Fifteen suppliers are listed for this compound. Additional details are available on the methylprednisolone sodium succinate profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for A-methapred
A generic version of A-METHAPRED was approved as methylprednisolone sodium succinate by FRESENIUS KABI USA on July 30th, 2004.
Summary for A-METHAPRED
US Patents: | 0 |
Applicants: | 3 |
NDAs: | 14 |
Raw Ingredient (Bulk) Api Vendors: | 19 |
Patent Applications: | 302 |
Formulation / Manufacturing: | see details |
DailyMed Link: | A-METHAPRED at DailyMed |
Anatomical Therapeutic Chemical (ATC) Classes for A-METHAPRED
US Patents and Regulatory Information for A-METHAPRED
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Abbott | A-METHAPRED | methylprednisolone sodium succinate | INJECTABLE;INJECTION | 089576-001 | Feb 22, 1991 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Hospira | A-METHAPRED | methylprednisolone sodium succinate | INJECTABLE;INJECTION | 040664-001 | Dec 20, 2005 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Abbott | A-METHAPRED | methylprednisolone sodium succinate | INJECTABLE;INJECTION | 089575-001 | Feb 22, 1991 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
>Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |