METHSCOPOLAMINE Drug Patent Profile
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When do Methscopolamine patents expire, and what generic alternatives are available?
Methscopolamine is a drug marketed by Breckenridge Pharm, Chartwell Rx, Ne Rx Pharma, Pvt Form, and Unichem. and is included in five NDAs.
The generic ingredient in METHSCOPOLAMINE is methscopolamine bromide. There are seven drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the methscopolamine bromide profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Methscopolamine
A generic version of METHSCOPOLAMINE was approved as methscopolamine bromide by BRECKENRIDGE PHARM on December 6th, 2011.
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Questions you can ask:
- What is the 5 year forecast for METHSCOPOLAMINE?
- What are the global sales for METHSCOPOLAMINE?
- What is Average Wholesale Price for METHSCOPOLAMINE?
Summary for METHSCOPOLAMINE
| US Patents: | 0 |
| Applicants: | 5 |
| NDAs: | 5 |
| Drug Prices: | Drug price information for METHSCOPOLAMINE |
| DailyMed Link: | METHSCOPOLAMINE at DailyMed |
US Patents and Regulatory Information for METHSCOPOLAMINE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Breckenridge Pharm | METHSCOPOLAMINE BROMIDE | methscopolamine bromide | TABLET;ORAL | 040642-001 | Dec 6, 2011 | AA | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| Pvt Form | METHSCOPOLAMINE BROMIDE | methscopolamine bromide | TABLET;ORAL | 080970-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Chartwell Rx | METHSCOPOLAMINE BROMIDE | methscopolamine bromide | TABLET;ORAL | 040624-002 | Dec 28, 2006 | DISCN | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | ||||
| Unichem | METHSCOPOLAMINE BROMIDE | methscopolamine bromide | TABLET;ORAL | 200602-001 | Sep 24, 2012 | AA | RX | No | No | ⤷ Start Trial | ⤷ Start Trial | ⤷ Start Trial | |||
| >Applicant | >Tradename | >Generic Name | >Dosage | >NDA | >Approval Date | >TE | >Type | >RLD | >RS | >Patent No. | >Patent Expiration | >Product | >Substance | >Delist Req. | >Exclusivity Expiration |
