NORTRIPTYLINE HYDROCHLORIDE Drug Patent Profile
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Which patents cover Nortriptyline Hydrochloride, and when can generic versions of Nortriptyline Hydrochloride launch?
Nortriptyline Hydrochloride is a drug marketed by Ani Pharms, Aurobindo Pharma Ltd, Dr Reddys Labs Sa, Rising, Taro, Teva, Zydus, Pharm Assoc, and Rubicon. and is included in eleven NDAs.
The generic ingredient in NORTRIPTYLINE HYDROCHLORIDE is nortriptyline hydrochloride. There are twelve drug master file entries for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the nortriptyline hydrochloride profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Nortriptyline Hydrochloride
A generic version of NORTRIPTYLINE HYDROCHLORIDE was approved as nortriptyline hydrochloride by DR REDDYS LABS SA on March 30th, 1992.
Summary for NORTRIPTYLINE HYDROCHLORIDE
US Patents: | 0 |
Applicants: | 9 |
NDAs: | 11 |
Finished Product Suppliers / Packagers: | 27 |
Raw Ingredient (Bulk) Api Vendors: | 92 |
Clinical Trials: | 50 |
Patent Applications: | 1,473 |
Formulation / Manufacturing: | see details |
DailyMed Link: | NORTRIPTYLINE HYDROCHLORIDE at DailyMed |
Recent Clinical Trials for NORTRIPTYLINE HYDROCHLORIDE
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Chang Gung Memorial Hospital | Phase 2 |
Assiut University | N/A |
Universidade do Extremo Sul Catarinense - Unidade Academica de Ciecias da Saude | Phase 2 |
Pharmacology for NORTRIPTYLINE HYDROCHLORIDE
Drug Class | Tricyclic Antidepressant |
Medical Subject Heading (MeSH) Categories for NORTRIPTYLINE HYDROCHLORIDE
Anatomical Therapeutic Chemical (ATC) Classes for NORTRIPTYLINE HYDROCHLORIDE
US Patents and Regulatory Information for NORTRIPTYLINE HYDROCHLORIDE
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Zydus | NORTRIPTYLINE HYDROCHLORIDE | nortriptyline hydrochloride | CAPSULE;ORAL | 213441-004 | Feb 24, 2021 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Teva | NORTRIPTYLINE HYDROCHLORIDE | nortriptyline hydrochloride | CAPSULE;ORAL | 074132-004 | Mar 27, 1995 | AB | RX | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | |||
Pharm Assoc | NORTRIPTYLINE HYDROCHLORIDE | nortriptyline hydrochloride | SOLUTION;ORAL | 075606-001 | Aug 23, 2000 | AA | RX | No | Yes | ⤷ 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 |