Details for New Drug Application (NDA): 062926
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The generic ingredient in RUBEX is doxorubicin hydrochloride. There are seventeen drug master file entries for this compound. Sixteen suppliers are listed for this compound. Additional details are available on the doxorubicin hydrochloride profile page.
Summary for 062926
Tradename: | RUBEX |
Applicant: | Bristol Myers Squibb |
Ingredient: | doxorubicin hydrochloride |
Patents: | 0 |
Medical Subject Heading (MeSH) Categories for 062926
Profile for product number 001
Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 10MG/VIAL | ||||
Approval Date: | Apr 13, 1989 | TE: | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 50MG/VIAL | ||||
Approval Date: | Apr 13, 1989 | TE: | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | DISCN | Dosage: | INJECTABLE;INJECTION | Strength | 100MG/VIAL | ||||
Approval Date: | Apr 13, 1989 | TE: | RLD: | No |
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