ETHAMBUTOL Drug Patent Profile
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When do Ethambutol patents expire, and when can generic versions of Ethambutol launch?
Ethambutol is a drug marketed by Barr, Epic Pharma Llc, and Lupin. and is included in three NDAs.
The generic ingredient in ETHAMBUTOL is ethambutol hydrochloride. There are five drug master file entries for this compound. Six suppliers are listed for this compound. Additional details are available on the ethambutol hydrochloride profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Ethambutol
A generic version of ETHAMBUTOL was approved as ethambutol hydrochloride by EPIC PHARMA LLC on November 30th, 1999.
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Questions you can ask:
- What is the 5 year forecast for ETHAMBUTOL?
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- What is Average Wholesale Price for ETHAMBUTOL?
Summary for ETHAMBUTOL
| US Patents: | 0 |
| Applicants: | 3 |
| NDAs: | 3 |
| Drug Prices: | Drug price information for ETHAMBUTOL |
| DailyMed Link: | ETHAMBUTOL at DailyMed |
US Patents and Regulatory Information for ETHAMBUTOL
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Barr | ETHAMBUTOL HYDROCHLORIDE | ethambutol hydrochloride | TABLET;ORAL | 076057-001 | Nov 26, 2001 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Lupin | ETHAMBUTOL HYDROCHLORIDE | ethambutol hydrochloride | TABLET;ORAL | 078939-001 | Jun 17, 2009 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Epic Pharma Llc | ETHAMBUTOL HYDROCHLORIDE | ethambutol hydrochloride | TABLET;ORAL | 075095-001 | Nov 30, 1999 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Epic Pharma Llc | ETHAMBUTOL HYDROCHLORIDE | ethambutol hydrochloride | TABLET;ORAL | 075095-002 | Nov 30, 1999 | AB | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Lupin | ETHAMBUTOL HYDROCHLORIDE | ethambutol hydrochloride | TABLET;ORAL | 078939-002 | Jun 17, 2009 | AB | RX | 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 |
