PERIOGARD Drug Patent Profile
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Which patents cover Periogard, and what generic alternatives are available?
Periogard is a drug marketed by Colgate Palmolive Co and Colgate-palmolive Co and is included in two NDAs.
The generic ingredient in PERIOGARD is chlorhexidine gluconate. There are fifty-eight drug master file entries for this compound. Fifty-six suppliers are listed for this compound. Additional details are available on the chlorhexidine gluconate profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Periogard
A generic version of PERIOGARD was approved as chlorhexidine gluconate by BECTON DICKINSON on October 24th, 1989.
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Questions you can ask:
- What is the 5 year forecast for PERIOGARD?
- What are the global sales for PERIOGARD?
- What is Average Wholesale Price for PERIOGARD?
Summary for PERIOGARD
US Patents: | 0 |
Applicants: | 2 |
NDAs: | 2 |
Finished Product Suppliers / Packagers: | 3 |
Raw Ingredient (Bulk) Api Vendors: | 42 |
Clinical Trials: | 7 |
Patent Applications: | 6,899 |
Drug Prices: | Drug price information for PERIOGARD |
DailyMed Link: | PERIOGARD at DailyMed |
Recent Clinical Trials for PERIOGARD
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
University of North Carolina, Chapel Hill | Phase 2 |
Colgate Palmolive | Phase 2 |
Universidade Estadual Paulista JĂșlio de Mesquita Filho | Phase 2/Phase 3 |
Pharmacology for PERIOGARD
Physiological Effect | Decreased Cell Wall Integrity |
US Patents and Regulatory Information for PERIOGARD
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Colgate Palmolive Co | PERIOGARD | chlorhexidine gluconate | SOLUTION;DENTAL | 073695-001 | Jan 14, 1994 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Colgate-palmolive Co | PERIOGARD | chlorhexidine gluconate | SOLUTION;DENTAL | 203212-001 | Jan 28, 2016 | AT | RX | 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 |