KANAMYCIN SULFATE - Generic Drug Details
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What are the generic sources for kanamycin sulfate and what is the scope of freedom to operate?
Kanamycin sulfate
is the generic ingredient in four branded drugs marketed by Apothecon, Hikma, Abraxis Pharm, Fresenius Kabi Usa, Intl Medication, Loch, Pharmafair, Solopak, Warner Chilcott, Watson Labs, and King Pharms, and is included in twenty NDAs. Additional information is available in the individual branded drug profile pages.There are five drug master file entries for kanamycin sulfate.
Summary for KANAMYCIN SULFATE
| US Patents: | 0 |
| Tradenames: | 4 |
| Applicants: | 11 |
| NDAs: | 20 |
| Drug Master File Entries: | 5 |
| Raw Ingredient (Bulk) Api Vendors: | 143 |
| Patent Applications: | 3,397 |
| DailyMed Link: | KANAMYCIN SULFATE at DailyMed |
Medical Subject Heading (MeSH) Categories for KANAMYCIN SULFATE
Anatomical Therapeutic Chemical (ATC) Classes for KANAMYCIN SULFATE
US Patents and Regulatory Information for KANAMYCIN SULFATE
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | TE | Type | RLD | RS | Patent No. | Patent Expiration | Product | Substance | Delist Req. | Exclusivity Expiration |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Fresenius Kabi Usa | KANAMYCIN SULFATE | kanamycin sulfate | INJECTABLE;INJECTION | 065111-001 | Dec 17, 2002 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Apothecon | KANTREX | kanamycin sulfate | INJECTABLE;INJECTION | 061901-003 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Apothecon | KANTREX | kanamycin sulfate | INJECTABLE;INJECTION | 061655-003 | Approved Prior to Jan 1, 1982 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Apothecon | KANTREX | kanamycin sulfate | INJECTABLE;INJECTION | 062564-003 | Sep 21, 1984 | DISCN | No | No | ⤷ Sign Up | ⤷ Sign Up | ⤷ Sign Up | ||||
| Pharmafair | KANAMYCIN SULFATE | kanamycin sulfate | INJECTABLE;INJECTION | 062669-001 | May 7, 1987 | 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 |
