Sold as Velban. Every FDA application for this active ingredient: 1 branded and 6 generic.
As of Nov 15, 2026, FDA lists 7 applications for Vinblastine Sulfate (sold as Velban), first approved Nov 25, 1965, with 0 new uses approved and 0 published complete response letters.
| Vinblastine Sulfate | Part B | $93K | -1% | 302 |
| Vinblastine Sulfate | Part D | $2K | +57% | 0 |
| Phase II Study Of Nivolumab Plus AVD In Pediatric, Adolescent, And Young Adult Patients With CHLHodgkin Lymphoma · M.D. Anderson Cancer Center | Phase 2 | Recruiting | Apr 27, 2026 |
| Modified LCH-III Regimen With or Without Luvometinib for Multisystem Pediatric Langerhans Cell HistiocytosisLangerhans Cell Histiocytosis (LCH) · West China Second University Hospital | Not applicable | Recruiting | Feb 24, 2026 |
| Comparison of AVD + Low-Dose Nivolumab vs. PET-Adapted BEACOPP-like in Advanced cHLHodgkin Lymphoma · St. Petersburg State Pavlov Medical University | Phase 2 | Recruiting | Nov 18, 2025 |
| PET-Adapted First-Line Therapy With Nivolumab for Advanced Hodgkin LymphomaHodgkin Lymphoma, Hodgkin Disease · National Research Center for Hematology, Russia | Phase 2 | Recruiting | Oct 6, 2025 |
| Effect of Neoadjuvant Chemotherapy on MRI Accuracy Before CystectomyMuscle Invasive Bladder Cancer · Assiut University | Not applicable | Recruiting | Oct 2, 2025 |
| Chemoimmunotherapy for ALK+ Relapsed/Refractory ALCLAnaplastic Large Cell Lymphoma, ALK-Positive · New York Medical College | Phase 2 | Recruiting | Jun 10, 2025 |
| Nivo40-AVD for Advanced Classic Hodgkin LymphomaHodgkin Lymphoma, Adult · National Medical Research Radiological Centre of the Ministry of Health of Russia | Phase 2 | Recruiting | May 22, 2025 |
| Perioperative Durvalumab With Neoadjuvant ddMVAC in Patients With Muscle-Invasive Bladder Cancer (NIAGARA-2)Urinary Bladder Neoplasms, Immune Checkpoint Inhibitors · AstraZeneca | Phase 2 | Recruiting | May 7, 2025 |
| Nov 25, 1965 | VelbanNDA 12665 · New molecular entity | Lilly | 34 | Discontinued |
| Apr 9, 1987 | Vinblastine SulfateANDA 89395 | Hikma | 9 | Marketed |
| Apr 29, 1987 | Vinblastine SulfateANDA 89515 | Fresenius Kabi USA | 16 | Marketed |
| Aug 18, 1987 | Vinblastine SulfateANDA 89565 | Hospira | 19 | Discontinued |
| — | Vinblastine SulfateANDA 89011 | Abraxis Pharm | 0 | Discontinued |
| — | Vinblastine SulfateANDA 89311 | Quad Pharms | 0 | Discontinued |
| — | Vinblastine SulfateANDA 89365 | Quad Pharms | 0 | Discontinued |
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient. Drugs@FDA