AMITID Drug Patent Profile
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Which patents cover Amitid, and when can generic versions of Amitid launch?
Amitid is a drug marketed by Bristol Myers Squibb and is included in one NDA.
The generic ingredient in AMITID is amitriptyline hydrochloride. There are thirteen drug master file entries for this compound. Forty-one suppliers are listed for this compound. Additional details are available on the amitriptyline hydrochloride profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Amitid
A generic version of AMITID was approved as amitriptyline hydrochloride by SUN PHARM INDS INC on July 14th, 1987.
Summary for AMITID
US Patents: | 0 |
Applicants: | 1 |
NDAs: | 1 |
Raw Ingredient (Bulk) Api Vendors: | 124 |
Patent Applications: | 2,894 |
Formulation / Manufacturing: | see details |
DailyMed Link: | AMITID at DailyMed |
Anatomical Therapeutic Chemical (ATC) Classes for AMITID
US Patents and Regulatory Information for AMITID
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Bristol Myers Squibb | AMITID | amitriptyline hydrochloride | TABLET;ORAL | 086454-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Bristol Myers Squibb | AMITID | amitriptyline hydrochloride | TABLET;ORAL | 086454-004 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Bristol Myers Squibb | AMITID | amitriptyline hydrochloride | TABLET;ORAL | 086454-002 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Bristol Myers Squibb | AMITID | amitriptyline hydrochloride | TABLET;ORAL | 086454-003 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Bristol Myers Squibb | AMITID | amitriptyline hydrochloride | TABLET;ORAL | 086454-005 | Approved Prior to Jan 1, 1982 | DISCN | No | 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 |