Procaine hydrochloride; tetracycline hydrochloride - Generic Drug Details
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What are the generic sources for procaine hydrochloride; tetracycline hydrochloride and what is the scope of freedom to operate?
Procaine hydrochloride; tetracycline hydrochloride
is the generic ingredient in two branded drugs marketed by Lederle and Pfizer, and is included in two NDAs. Additional information is available in the individual branded drug profile pages.Summary for procaine hydrochloride; tetracycline hydrochloride
US Patents: | 0 |
Tradenames: | 2 |
Applicants: | 2 |
NDAs: | 2 |
Clinical Trials: | 1 |
DailyMed Link: | procaine hydrochloride; tetracycline hydrochloride at DailyMed |
Recent Clinical Trials for procaine hydrochloride; tetracycline hydrochloride
Identify potential brand extensions & 505(b)(2) entrants
Sponsor | Phase |
---|---|
Alphacait, LLC | Phase 2 |
Haining Health-Coming Biotech Co., Ltd. | Phase 2 |
See all procaine hydrochloride; tetracycline hydrochloride clinical trials
Anatomical Therapeutic Chemical (ATC) Classes for procaine hydrochloride; tetracycline hydrochloride
US Patents and Regulatory Information for procaine hydrochloride; tetracycline hydrochloride
Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Pfizer | TETRACYN | procaine hydrochloride; tetracycline hydrochloride | INJECTABLE;INJECTION | 060285-003 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Lederle | ACHROMYCIN | procaine hydrochloride; tetracycline hydrochloride | INJECTABLE;INJECTION | 050276-003 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
Pfizer | TETRACYN | procaine hydrochloride; tetracycline hydrochloride | INJECTABLE;INJECTION | 060285-002 | 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 |