Last Updated: June 23, 2026

PRED Drug Patent Profile


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When do Pred patents expire, and what generic alternatives are available?

Pred is a drug marketed by Abbvie, Allergan, Pharmafair, Epic Pharma Llc, Fougera Pharms, Schwarz Pharma, Chartwell Rx, Hikma, Ivax Sub Teva Pharms, Lannett Co Inc, Nesher Pharms, Pharm Assoc, Pharmobedient Cnsltg, Teva Pharms, Tp Anda Holdings, We Pharms, Aurobindo Pharma Ltd, Barr, Bundy, Chartwell Molecular, Elkins Sinn, Everylife, Ferrante, Fosun Pharma, Heather, Impax Labs, Inwood Labs, Marshall Pharma, Panray, Phoenix Labs Ny, Purepac Pharm, Pvt Form, Rising, Roxane, Sperti, Superpharm, Tablicaps, Teva, UDL, Valeant Pharm Intl, Vitarine, Watson Labs, West Ward, Whiteworth Town Plsn, Zhejiang Xianju, Bel Mar, Cent Pharms, Amneal, Lupin, Alcon Pharms Ltd, Bausch And Lomb, Sola Barnes Hind, Amneal Pharms, Bausch, Edenbridge Pharms, Mission Pharma, Ph Health, Pharmobedient, Vintage Pharms, Xttrium Labs Inc, Actavis Labs Fl Inc, Dr Reddys, Aiping Pharm Inc, Am Therap, Amneal Pharms Ny, Contract Pharmacal, Duramed Pharms Barr, Geneyork Pharms, Halsey, Hikma Pharms, Jubilant Cadista, Kv Pharm, Lederle, Mutual Pharm, Mylan, Novitium Pharma, Nylos, Pharmavite, Pointview Hldings, Rexall, Scherer Labs, Strides Pharma, Sun Pharm Industries, Upsher Smith, and Vangard. and is included in two hundred and twelve NDAs.

The generic ingredient in PRED is prednisolone tebutate. There are eighty-eight drug master file entries for this compound. Additional details are available on the prednisolone tebutate profile page.

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Summary for PRED

US Patents and Regulatory Information for PRED

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Watson Labs PREDNISOLONE ACETATE prednisolone acetate INJECTABLE;INJECTION 083767-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Strides Pharma PREDNISONE prednisone TABLET;ORAL 208412-001 Feb 11, 2021 AB RX No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Pharm Assoc PREDNISOLONE SODIUM PHOSPHATE prednisolone sodium phosphate SOLUTION;ORAL 076123-001 Dec 23, 2002 DISCN No No ⤷  Start Trial ⤷  Start Trial ⤷  Start Trial
Udl PREDNISONE prednisone TABLET;ORAL 087986-001 Jan 18, 1983 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

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. We do not provide individual investment advice. This service is not registered with any financial regulatory agency. The information we publish is educational only and based on our opinions plus our models. By using DrugPatentWatch you acknowledge that we do not provide personalized recommendations or advice. thinkBiotech performs no independent verification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.