approval
saveMAGNESIUM SULFATE — FDA approval
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Sponsor: BAXTER HLTHCARE CORP. Form: INJECTABLE. Route: INJECTION
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drug timeline · 8
- approvalSUPREP BOWEL PREP KIT (MAGNESIUM SULFATE) — FDA approvalNov 18, 2025 · 317d ago
- approvalMAGNESIUM SULFATE — FDA approvalMay 10, 2022 · 1605d ago
- approvalSUPREP BOWEL PREP KIT (MAGNESIUM SULFATE) — FDA approvalAug 5, 2020 · 2248d ago
- approvalMAGNESIUM SULFATE — FDA approvalJun 1, 2020 · 2313d ago
- approvalSUPREP BOWEL PREP KIT (MAGNESIUM SULFATE) — FDA approvalNov 6, 2012 · 5077d ago
- approvalSUPREP BOWEL PREP KIT (MAGNESIUM SULFATE) — FDA approvalJul 24, 2012 · 5182d ago
- approvalSUPREP BOWEL PREP KIT (MAGNESIUM SULFATE) — FDA approvalJul 6, 2011 · 5566d ago
- approvalSUPREP BOWEL PREP KIT (MAGNESIUM SULFATE) — FDA approvalAug 5, 2010 · 5901d ago
same company · ±60 days · 6
- device recallBaxter Healthcare Corporation device recall (Cls II)Jan 13, 2026
- device 510kBaxter Healthcare Corp/ Excel Medical — WAVE Clinical Platform (2.0.000) (510k cleared)Jan 16, 2026
- device 510kBaxter Healthcare Corporation — Welch Allyn FlexiPort Blood Pressure Cuffs (FlexiPort Blood Pressure Cuffs) (510k cleared)Dec 16, 2025
- recallBaxter Healthcare Corporation recall (Cls II)Feb 4, 2026
- approvalNOREPINEPHRINE BITARTRATE: NOREPINEPHRINE BITARTRATE IN 0.9% SODIUM CHLORIDE (NOREPINEPHRINE BITARTRATE) — FDA approvalFeb 6, 2026
- device recallBaxter Healthcare Corporation device recall (Cls I)Feb 18, 2026
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