TOBRAMYCIN (TOBRAMYCIN SULFATE)
Summary
FDA approved TOBRAMYCIN (TOBRAMYCIN SULFATE) by FRESENIUS KABI USA. NDA (New Drug) approval (Labeling) on 2023-02-10. INJECTABLE, INJECTION.
Details
Source
Drug Approval
External ID
NDA050789-17
Action Date
2023-02-10
Status
Approved
Category
drug
Product Code
NDA (New Drug)
Product Description
TOBRAMYCIN (generic: TOBRAMYCIN SULFATE), INJECTABLE, INJECTION. Application: NDA050789
Company
Context & Analysis
FRESENIUS KABI USA has 70 FDA actions in our database.
Frequently Asked Questions
How often does FRESENIUS KABI USA have FDA actions?
FRESENIUS KABI USA has 70 FDA actions in our database, including 0 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "NDA050789-17" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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