PROCAN SR Drug Patent Profile
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When do Procan Sr patents expire, and what generic alternatives are available?
Procan Sr is a drug marketed by Parke Davis and Parkedale and is included in four NDAs.
The generic ingredient in PROCAN SR is procainamide hydrochloride. There are nine drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the procainamide hydrochloride profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Procan Sr
A generic version of PROCAN SR was approved as procainamide hydrochloride by INTL MEDICATION on July 31st, 1984.
Summary for PROCAN SR
US Patents: | 0 |
Applicants: | 2 |
NDAs: | 4 |
Raw Ingredient (Bulk) Api Vendors: | 119 |
Clinical Trials: | 1 |
Patent Applications: | 1,256 |
Formulation / Manufacturing: | see details |
DailyMed Link: | PROCAN SR at DailyMed |
Recent Clinical Trials for PROCAN SR
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Evan Adelstein, MD | N/A |
UPMC | N/A |
University of Pittsburgh | N/A |
Anatomical Therapeutic Chemical (ATC) Classes for PROCAN SR
US Patents and Regulatory Information for PROCAN SR
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Parke Davis | PROCAN SR | procainamide hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 086468-001 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Parkedale | PROCAN SR | procainamide hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 087510-001 | Apr 1, 1982 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Parkedale | PROCAN SR | procainamide hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 088489-001 | Jan 16, 1985 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Parkedale | PROCAN SR | procainamide hydrochloride | TABLET, EXTENDED RELEASE;ORAL | 086065-001 | Approved Prior to Jan 1, 1982 | DISCN | Yes | 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 |