FENTANYL CITRATE PRESERVATIVE FREE Drug Patent Profile
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When do Fentanyl Citrate Preservative Free patents expire, and what generic alternatives are available?
Fentanyl Citrate Preservative Free is a drug marketed by Dr Reddys, Fresenius Kabi Usa, and Hospira. and is included in three NDAs.
The generic ingredient in FENTANYL CITRATE PRESERVATIVE FREE is fentanyl citrate. There are thirty-one drug master file entries for this compound. Ten suppliers are listed for this compound. Additional details are available on the fentanyl citrate profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Fentanyl Citrate Preservative Free
A generic version of FENTANYL CITRATE PRESERVATIVE FREE was approved as fentanyl citrate by HIKMA on July 11th, 1984.
Summary for FENTANYL CITRATE PRESERVATIVE FREE
US Patents: | 0 |
Applicants: | 3 |
NDAs: | 3 |
Finished Product Suppliers / Packagers: | 1 |
Raw Ingredient (Bulk) Api Vendors: | 38 |
Formulation / Manufacturing: | see details |
DailyMed Link: | FENTANYL CITRATE PRESERVATIVE FREE at DailyMed |
Pharmacology for FENTANYL CITRATE PRESERVATIVE FREE
Drug Class | Opioid Agonist |
Mechanism of Action | Full Opioid Agonists |
Anatomical Therapeutic Chemical (ATC) Classes for FENTANYL CITRATE PRESERVATIVE FREE
US Patents and Regulatory Information for FENTANYL CITRATE PRESERVATIVE FREE
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Dr Reddys | FENTANYL CITRATE PRESERVATIVE FREE | fentanyl citrate | INJECTABLE;INJECTION | 074917-001 | Feb 3, 1998 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Fresenius Kabi Usa | FENTANYL CITRATE PRESERVATIVE FREE | fentanyl citrate | INJECTABLE;INJECTION | 210762-001 | May 3, 2019 | AP | RX | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | |||
Hospira | FENTANYL CITRATE PRESERVATIVE FREE | fentanyl citrate | INJECTABLE;INJECTION | 072786-001 | Sep 24, 1991 | AP | RX | 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 |