approval
saveNOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (NOREPINEPHRINE BITARTRATE) — FDA approval
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Sponsor: BAXTER HLTHCARE CORP. Form: SOLUTION. Route: INTRAVENOUS
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drug timeline · 7
- approvalNOREPINEPHRINE BITARTRATE IN 5% DEXTROSE (NOREPINEPHRINE BITARTRATE) — FDA approvalMar 26, 2026 · 190d ago
- approvalNOREPINEPHRINE BITARTRATE — FDA approvalDec 11, 2025 · 295d ago
- approvalNOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (NOREPINEPHRINE BITARTRATE) — FDA approvalJun 11, 2024 · 843d ago
- approvalNOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (NOREPINEPHRINE BITARTRATE) — FDA approvalNov 23, 2023 · 1044d ago
- approvalNOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (NOREPINEPHRINE BITARTRATE) — FDA approvalJun 2, 2022 · 1583d ago
- approvalNOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (NOREPINEPHRINE BITARTRATE) — FDA approvalJun 2, 2022 · 1583d ago
- approvalNOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (NOREPINEPHRINE BITARTRATE) — FDA approvalJan 15, 2021 · 2086d ago
same company · ±60 days · 6
- recallBaxter Healthcare Corporation recall (Cls II)Feb 4, 2026
- device recallBaxter Healthcare Corporation device recall (Cls II)Feb 18, 2026
- device recallBaxter Healthcare Corporation device recall (Cls I)Feb 18, 2026
- approvalPHYTONADIONE: PHYTONADIONE — FDA approvalFeb 26, 2026
- device 510kBaxter Healthcare Corp/ Excel Medical — WAVE Clinical Platform (2.0.000) (510k cleared)Jan 16, 2026
- device recallBaxter Healthcare Corporation device recall (Cls II)Jan 13, 2026
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