Last reviewed · How we verify
Mixtard® 30 TDS
Mixtard® 30 TDS is a Small molecule drug developed by Hospital Sultanah Aminah Johor Bahru. It is currently FDA-approved.
At a glance
| Generic name | Mixtard® 30 TDS |
|---|---|
| Sponsor | Hospital Sultanah Aminah Johor Bahru |
| Modality | Small molecule |
| Phase | FDA-approved |
Approved indications
Common side effects
Key clinical trials
Primary sources
Every claim on this page is sourced from regulatory or scientific primary sources. See our editorial policy for full methodology.
| Source | Used for |
|---|---|
| ClinicalTrials.gov | Trial enrolment, design, endpoints, results |
Competitive intelligence
For the full competitive landscape — auto-detected comparators, recent regulatory actions across the set, upcoming PDUFA, patent timeline, sponsor landscape:
- Mixtard® 30 TDS CI brief — competitive landscape report
- Mixtard® 30 TDS updates RSS · CI watch RSS
- Hospital Sultanah Aminah Johor Bahru portfolio CI
Frequently asked questions about Mixtard® 30 TDS
What is Mixtard® 30 TDS?
Mixtard® 30 TDS is a Small molecule drug developed by Hospital Sultanah Aminah Johor Bahru.
Who makes Mixtard® 30 TDS?
Mixtard® 30 TDS is developed and marketed by Hospital Sultanah Aminah Johor Bahru (see full Hospital Sultanah Aminah Johor Bahru pipeline at /company/hospital-sultanah-aminah-johor-bahru).
What development phase is Mixtard® 30 TDS in?
Mixtard® 30 TDS is FDA-approved (marketed).
Related
- Manufacturer: Hospital Sultanah Aminah Johor Bahru — full pipeline
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing