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calendar

28 catalysts · 14 approval · 8 device recall · 3 device 510k · 2 grant · 1 device pma

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therapy area

no tagged catalysts yet

Week of Jan 26, 2026

28
›Jan 26, 2026approval215d agoAMLODIPINE BESYLATE — FDA approvalGraviti Pharmaceuticals Inc

Sponsor: GRAVITI PHARMS. Form: TABLET. Route: ORAL

full page →fda approvals ↗
›Jan 26, 2026approval215d agoBETAMETHASONE DIPROPIONATE — FDA approvalBETAMETHASONE DIPROPIONATE

Sponsor: AUROBINDO PHARMA LTD. Form: CREAM. Route: TOPICAL

full page →BETAMETHASONE DIPROPIONATE →fda approvals ↗
›Jan 26, 2026approval215d agoPALIPERIDONE — FDA approvalpaliperidone ER

Sponsor: APOTEX. Form: TABLET, EXTENDED RELEASE. Route: ORAL

full page →paliperidone ER →fda approvals ↗
›Jan 26, 2026approval215d agoMETHYLPREDNISOLONE ACETATE — FDA approvalPFIZER INC

Sponsor: CAPLIN. Form: INJECTABLE. Route: INJECTION

full page →fda approvals ↗
›Jan 26, 2026approval215d agoDOXYCYCLINE HYCLATE — FDA approvalDOXYCYCLINE HYCLATE

Sponsor: AMNEAL. Form: TABLET. Route: ORAL

full page →DOXYCYCLINE HYCLATE →fda approvals ↗
›Jan 26, 2026approval215d agoFINASTERIDE — FDA approvalTeva Pharmaceuticals USA Inc

Sponsor: TEVA. Form: TABLET. Route: ORAL

full page →fda approvals ↗
›Jan 26, 2026approval215d agoCHLORPROMAZINE HYDROCHLORIDE — FDA approvalCHLORPROMAZINE HYDROCHLORIDE

Sponsor: MSN. Form: INJECTABLE. Route: INJECTION

full page →CHLORPROMAZINE HYDROCHLORIDE →fda approvals ↗
›Jan 26, 2026approval215d agoTRANEXAMIC ACID — FDA approvalHyloris Pharmaceuticals SA

Sponsor: I 3 PHARMS. Form: TABLET. Route: ORAL

full page →fda approvals ↗
›Jan 26, 2026approval215d agoDIFLUPREDNATE — FDA approvalDIFLUPREDNATE

Sponsor: ALEMBIC. Form: EMULSION. Route: OPHTHALMIC

full page →DIFLUPREDNATE →fda approvals ↗
›Jan 26, 2026approval215d agoTAPENTADOL HYDROCHLORIDE — FDA approvaltapentadol hydrochloride ER

Sponsor: NOVITIUM PHARMA. Form: SOLUTION. Route: ORAL

full page →tapentadol hydrochloride ER →fda approvals ↗
›Jan 26, 2026approval215d agoDAPTOMYCIN — FDA approvalDaptomycin Novo

Sponsor: ACCORD HLTHCARE. Form: POWDER. Route: INTRAVENOUS

full page →Daptomycin Novo →fda approvals ↗
›Jan 26, 2026approval215d agoBUDESONIDE — FDA approvalbudesonide DR

Sponsor: RISING. Form: CAPSULE, DELAYED RELEASE. Route: ORAL

full page →budesonide DR →fda approvals ↗
›Jan 26, 2026approval215d agoQUIOFIC (FOLIC ACID) — FDA approvalfolic acid

Sponsor: SOLUBIOMIX. Form: SOLUTION. Route: ORAL

full page →folic acid →fda approvals ↗
›Jan 26, 2026approval215d agoCUPRIC CHLORIDE — FDA approvalCUPRIC CHLORIDE

Sponsor: AMNEAL. Form: INJECTABLE. Route: INJECTION

full page →CUPRIC CHLORIDE →fda approvals ↗
›Jan 26, 2026device 510k215d agoOutset Medical, Inc. — Tablo Hemodialysis System (PN-0008000, PN-0006000U) (510k cleared)Outset Medical, Inc.

Product code: KDI. Advisory committee: Gastroenterology, Urology. Type: Traditional

full page →fda device 510k ↗
›Jan 26, 2026device 510k215d agoEyas Medical Imaging, Inc. — Ascent3T Neonatal Magnetic Resonance Imaging System (510k cleared)

Product code: LNH. Advisory committee: Radiology. Type: Traditional

full page →fda device 510k ↗
›Jan 26, 2026device 510k215d agoGe Medical Systems Information Technologies, Inc. — MAC 7 Resting ECG Analysis System (510k cleared)

Product code: DPS. Advisory committee: Cardiovascular. Type: Traditional

full page →fda device 510k ↗
›Jan 26, 2026device pma215d agoDiaSorin, Inc. — LIAISON QuantiFERON TB Gold Plus II; LIAISON Control QuantiFERON TB Gold Plus II (PMA supplement)

Supplement type: Normal 180 Day Track. Product code: NCD. Advisory committee: MI. Decision: APPR

full page →fda device pma ↗
›Jan 26, 2026device recall215d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

Azurion 7 M12 System Model Numbers: (1)722078, (2)722223, (3)722233; Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

full page →fda device recalls ↗
›Jan 26, 2026device recall215d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

Azurion 7 M20 System Model Numbers: (1)722079, (2)722224, (3)722234, (4)722282(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

full page →fda device recalls ↗
›Jan 26, 2026device recall215d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

Azurion 7 B12 System Model Numbers:(1) 722067, (2) 722225, (3) 722235; Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

full page →fda device recalls ↗
›Jan 26, 2026device recall215d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

Azurion 5 M12 System Model Numbers: (1)722227, (2)722231; Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

full page →fda device recalls ↗
›Jan 26, 2026device recall215d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

Azurion 3 M15 System Model Numbers: (1) 722064, (2) 722222, (3) 722230, (4)722280(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

full page →fda device recalls ↗
›Jan 26, 2026device recall215d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

Azurion 3 M12 System Model Numbers: (1) 722063, (2) 722221, (3) 722229; Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

full page →fda device recalls ↗
›Jan 26, 2026device recall215d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

Azurion 7 B20 System Model Numbers: (1)722068, (2)722226, (3)722236; Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

full page →fda device recalls ↗
›Jan 26, 2026device recall215d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

Azurion 5 M20 System Model Numbers: (1)722228, (2)722232, (3)722281(OUS only); Software Version Number - All versions: R1.X, R2.X, R3.X — Reason: Under certain conditions, the table may move unexpectedly when the Reset Geometry button is pressed - even when a table lock is active. — Status: Ongoing

full page →fda device recalls ↗
›Jan 26, 2026grant215d agoFLORIDA INTERNATIONAL UNIVERSITY — CRISPR/dCas9-Targeted Histone Demethylation Interplays with DNA Repair to Con...

NS grant. $1,319,674. PI: Prem P Chapagain

full page →nih reporter ↗
›Jan 26, 2026grant215d agoEMORY UNIVERSITY — Neuromodulation of somato-sympathetic postganglionic activity after SCIEmory University

NS grant. $234,750. PI: SHAWN HOCHMAN

full page →nih reporter ↗
$AMRX17.99+0.39%
$AMRX17.99+0.39%
$PFE28.03-0.96%
$OM4.5200-1.09%