STROMECTOL Drug Patent Profile
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When do Stromectol patents expire, and what generic alternatives are available?
Stromectol is a drug marketed by Merck Sharp Dohme and is included in one NDA.
The generic ingredient in STROMECTOL is ivermectin. There are five drug master file entries for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the ivermectin profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Stromectol
A generic version of STROMECTOL was approved as ivermectin by EDENBRIDGE PHARMS on October 24th, 2014.
Summary for STROMECTOL
| US Patents: | 0 |
| Applicants: | 1 |
| NDAs: | 1 |
| Finished Product Suppliers / Packagers: | 1 |
| Raw Ingredient (Bulk) Api Vendors: | 4 |
| Clinical Trials: | 22 |
| Patent Applications: | 4 |
| Formulation / Manufacturing: | see details |
| Drug Prices: | Drug price information for STROMECTOL |
| What excipients (inactive ingredients) are in STROMECTOL? | STROMECTOL excipients list |
| DailyMed Link: | STROMECTOL at DailyMed |
Recent Clinical Trials for STROMECTOL
Identify potential brand extensions & 505(b)(2) entrants
| Sponsor | Phase |
|---|---|
| Galvita AG, Switzerland | Early Phase 1 |
| University Children's Hospital Basel | Early Phase 1 |
| Permamed AG, Switzerland | Early Phase 1 |
Pharmacology for STROMECTOL
| Drug Class | Antiparasitic Pediculicide |
Anatomical Therapeutic Chemical (ATC) Classes for STROMECTOL
US Patents and Regulatory Information for STROMECTOL
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Merck Sharp Dohme | STROMECTOL | ivermectin | TABLET;ORAL | 050742-002 | Oct 8, 1998 | AB | RX | Yes | Yes | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | |||
| Merck Sharp Dohme | STROMECTOL | ivermectin | TABLET;ORAL | 050742-001 | Nov 22, 1996 | 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 |
