Tedizolid Phosphate

CAS 856867-55-5 5 current recordsSmall Molecule

Who holds supplier records for Tedizolid Phosphate? 5 organisations hold a current record for Tedizolid Phosphate: an active US FDA Type II Drug Master File. Recorded organisation countries for current records: China (2) and India (2); not recorded for 1.

Sources: FDA Drug Master File list, EDQM certification database, FDA Orange Book. Record updated 3 Aug 2026. How we read these records

Reading the evidence

  • 5 current records

    Several organisations hold current DMFs or CEPs. Whether any is a usable source for your grade, scale and market still needs qualification.

  • No company-level GMP certificate matched

    No current EU or UK GMP certificate was matched to these organisations. That is not a negative finding; ask each candidate for its certificate and latest inspection outcome.

Current records (5)

Organisations holding an active US FDA Type II Drug Master File or a CEP for Tedizolid Phosphate. Country is the organisation's recorded country, not necessarily the manufacturing site.

China2India2Country not recorded for 1
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Overview

Tedizolid Phosphate is a small molecule active pharmaceutical ingredient (ChEMBL CHEMBL2105669).

Chemical identity

IUPAC name
[(5R)-3-[3-fluoro-4-[6-(2-methyltetrazol-5-yl)-3-pyridinyl]phenyl]-2-oxo-1,3-oxazolidin-5-yl]methyl dihydrogen phosphate
Canonical SMILES
CN1N=C(N=N1)C2=NC=C(C=C2)C3=C(C=C(C=C3)N4C[C@@H](OC4=O)COP(=O)(O)O)F
InChIKey
QCGUSIANLFXSGE-GFCCVEGCSA-N
Synonyms
Sivextro, Tedizolid phosphate, TR-701 FA, TR-701-FA, TR-701FA, Torezolid phosphate, CHEBI:83326, DA7218, RefChem:56098, Tedizolid phosphate [USAN], Tedizolid (phosphate), TedizolidPhosphate

Record history

PharmaTek records which organisations hold a current DMF or CEP for Tedizolid Phosphate every week, starting 23 Oct 2026. Additions and lapses will appear here from the next weekly release.

Monitoring pilot: get an email when these records change. Places are confirmed by a person; nothing is sent until then. All changes this week

What these records establish

  • An active DMF means a confidential file is held by the FDA and can be referenced; the FDA does not approve or disapprove DMFs.
  • A CEP confirms monograph suitability for the EU market; it is not a GMP certificate, and the holder may not be the manufacturer.
  • Historical records show a past filing, not current supply.
  • Company GMP certificates are matched to the organisation, not to the site making this substance.
  • A substance missing from these registers is not evidence that no supplier exists.

Frequently asked questions

Which organisations hold current supplier records for Tedizolid Phosphate?

5 organisations hold an active US FDA Type II Drug Master File or a CEP for Tedizolid Phosphate: ALP PHARM BEIJING CO LTD, ANHUI BIOCOMPOUNDS PHARMACEUTICAL CO LTD (China), Arene Life Sciences Limited (India), METROCHEM API PRIVATE LTD (India) and Shanghai Desano Chemical Pharmaceutical Co., Ltd (China). A DMF or CEP shows a regulatory filing, not current commercial availability, and the holder is not necessarily the manufacturing site.

Which Tedizolid Phosphate Drug Master Files are active?

ALP PHARM BEIJING CO LTD (DMF 41850), ANHUI BIOCOMPOUNDS PHARMACEUTICAL CO LTD (DMF 39381), Arene Life Sciences Limited (DMF 42648), METROCHEM API PRIVATE LTD (DMF 35515) and Shanghai Desano Chemical Pharmaceutical Co., Ltd (DMF 40498). The FDA does not approve or disapprove DMFs; an active DMF can be referenced in an application once its holder issues a letter of authorisation.

How do I qualify a Tedizolid Phosphate supplier?

Confirm the DMF or CEP is current and covers your grade, obtain the letter of authorisation, identify the actual manufacturing site and check its GMP certificate and FDA inspection history, audit the site or review a recent audit, and run comparable requests for information across more than one candidate.

For suppliers

Do you supply Tedizolid Phosphate?

Send a link to a certificate, registration or filing we have missed or got wrong. We check it against the issuing register before changing anything; information we cannot check against a register is shown as supplier-reported.

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