CECLOR Drug Patent Profile
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When do Ceclor patents expire, and what generic alternatives are available?
Ceclor is a drug marketed by Lilly and is included in three NDAs.
The generic ingredient in CECLOR is cefaclor. There are thirteen drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the cefaclor profile page.
DrugPatentWatch® Litigation and Generic Entry Outlook for Ceclor
A generic version of CECLOR was approved as cefaclor by TEVA on September 4th, 2002.
Summary for CECLOR
US Patents: | 0 |
Applicants: | 1 |
NDAs: | 3 |
Raw Ingredient (Bulk) Api Vendors: | 78 |
Patent Applications: | 5,207 |
Formulation / Manufacturing: | see details |
DailyMed Link: | CECLOR at DailyMed |
Anatomical Therapeutic Chemical (ATC) Classes for CECLOR
US Patents and Regulatory Information for CECLOR
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Lilly | CECLOR | cefaclor | CAPSULE;ORAL | 050521-001 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Lilly | CECLOR | cefaclor | FOR SUSPENSION;ORAL | 050522-002 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Lilly | CECLOR | cefaclor | CAPSULE;ORAL | 050521-002 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Lilly | CECLOR | cefaclor | FOR SUSPENSION;ORAL | 050522-001 | Approved Prior to Jan 1, 1982 | DISCN | Yes | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Lilly | CECLOR CD | cefaclor | TABLET, EXTENDED RELEASE;ORAL | 050673-002 | Jun 28, 1996 | DISCN | No | No | ⤷ Try a Trial | ⤷ Try a Trial | ⤷ Try a Trial | ||||
Lilly | CECLOR CD | cefaclor | TABLET, EXTENDED RELEASE;ORAL | 050673-001 | Jun 28, 1996 | 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 |