
UB477
ProductDobutamine Injection
Strength250mg/20ml, 500mg/40ml
IndicationsCardiac decompensation; Cardiac failure acute; Cardiogenic shock
TherapeuticsCardiovascular
GMPUS - FDA
RegistrationUnited States
ModalitiesSmall Molecule
Exclusive Summary
- - Originator launched around 1978 with patents long expired; no active blocking IP, enabling fast global market entry and tender participation.
- - Stable ICU demand: ~64 million heart-failure patients worldwide, ~0.5–1.0 million cardiogenic-shock cases annually, plus millions of dobutamine stress-echocardiography tests.
- - Included in the WHO Essential Medicines List and recommended by AHA/ACC, ESC, and Sepsis guidelines for low cardiac output/hypoperfusion—standard hospital rescue therapy.
- - US registration (SRA-compliant) facilitates reliance/abridged approvals and accelerates uptake with strong compliance credentials.
- - Mature generics but supply fluctuations exist; with two practical strengths and reliable supply, the product can win tenders and deliver ~30–70% savings vs originator.
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