MAPROTILINE HYDROCHLORIDE Drug Patent Profile
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Which patents cover Maprotiline Hydrochloride, and what generic alternatives are available?
Maprotiline Hydrochloride is a drug marketed by Am Therap, Heritage Pharma, Rising, and Watson Labs. and is included in ten NDAs.
The generic ingredient in MAPROTILINE HYDROCHLORIDE is maprotiline hydrochloride. There are three drug master file entries for this compound. Additional details are available on the maprotiline hydrochloride profile page.
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Summary for MAPROTILINE HYDROCHLORIDE
| US Patents: | 0 |
| Applicants: | 4 |
| NDAs: | 10 |
| Raw Ingredient (Bulk) Api Vendors: | 110 |
| Clinical Trials: | 3 |
| Patent Applications: | 884 |
| DailyMed Link: | MAPROTILINE HYDROCHLORIDE at DailyMed |
Recent Clinical Trials for MAPROTILINE HYDROCHLORIDE
Identify potential brand extensions & 505(b)(2) entrants
| Sponsor | Phase |
|---|---|
| University of Rochester | Phase 1 |
| Hannover Medical School | Phase 3 |
| VA Office of Research and Development | Phase 2 |
Medical Subject Heading (MeSH) Categories for MAPROTILINE HYDROCHLORIDE
Anatomical Therapeutic Chemical (ATC) Classes for MAPROTILINE HYDROCHLORIDE
US Patents and Regulatory Information for MAPROTILINE HYDROCHLORIDE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Am Therap | MAPROTILINE HYDROCHLORIDE | maprotiline hydrochloride | TABLET;ORAL | 072129-001 | Jan 14, 1988 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Rising | MAPROTILINE HYDROCHLORIDE | maprotiline hydrochloride | TABLET;ORAL | 072285-001 | Oct 3, 1988 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Heritage Pharma | MAPROTILINE HYDROCHLORIDE | maprotiline hydrochloride | TABLET;ORAL | 072162-001 | Jun 1, 1988 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Watson Labs | MAPROTILINE HYDROCHLORIDE | maprotiline hydrochloride | TABLET;ORAL | 072164-001 | Jun 1, 1988 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
