AMITID Drug Patent Profile
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When do Amitid patents expire, and what generic alternatives are available?
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-three 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.
AI Research Assistant
Questions you can ask:
- What is the 5 year forecast for AMITID?
- What are the global sales for AMITID?
- What is Average Wholesale Price for AMITID?
Summary for AMITID
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 1 |
| Raw Ingredient (Bulk) Api Vendors: | 124 |
| Patent Applications: | 2,828 |
| DailyMed Link: | AMITID at DailyMed |
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 | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Bristol Myers Squibb | AMITID | amitriptyline hydrochloride | TABLET;ORAL | 086454-004 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Bristol Myers Squibb | AMITID | amitriptyline hydrochloride | TABLET;ORAL | 086454-002 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Bristol Myers Squibb | AMITID | amitriptyline hydrochloride | TABLET;ORAL | 086454-003 | Approved Prior to Jan 1, 1982 | 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 |
