Methacycline hydrochloride - Generic Drug Details
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What are the generic drug sources for methacycline hydrochloride and what is the scope of patent protection?
Methacycline hydrochloride
is the generic ingredient in one branded drug marketed by Medpointe Pharm Hlc and is included in one NDA. Additional information is available in the individual branded drug profile pages.There are four drug master file entries for methacycline hydrochloride.
Summary for methacycline hydrochloride
| US Patents: | 0 |
| Tradenames: | 1 |
| Applicants: | 1 |
| NDAs: | 1 |
| Drug Master File Entries: | 4 |
| Raw Ingredient (Bulk) Api Vendors: | 84 |
| Clinical Trials: | 1 |
| Patent Applications: | 1,605 |
| DailyMed Link: | methacycline hydrochloride at DailyMed |
Recent Clinical Trials for methacycline hydrochloride
Identify potential brand extensions & 505(b)(2) entrants
| Sponsor | Phase |
|---|---|
| University of Louisville | Early Phase 1 |
| James Graham Brown Cancer Center | Early Phase 1 |
| Julio Ramirez | Early Phase 1 |
Medical Subject Heading (MeSH) Categories for methacycline hydrochloride
US Patents and Regulatory Information for methacycline hydrochloride
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Medpointe Pharm Hlc | RONDOMYCIN | methacycline hydrochloride | CAPSULE;ORAL | 060641-001 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Medpointe Pharm Hlc | RONDOMYCIN | methacycline hydrochloride | SYRUP;ORAL | 060641-003 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Medpointe Pharm Hlc | RONDOMYCIN | methacycline hydrochloride | CAPSULE;ORAL | 060641-002 | 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 |
