Suppliers / Ctx Life Sciences

Ctx Life Sciences

India Updated 9 July 2026

The public registers hold a second record for Ctx Life Sciences. The fuller profile, with 27 active US DMFs and 21 valid CEPs, is at CTX Lifesciences. Figures on this page cover only this record.

Ctx Life Sciences is an API manufacturer based in India. It holds 17 active US drug master files across a filed portfolio of 16 molecules. Its GMP standing is certified by CDSCO (India).

17
active US DMFs
0
valid CEPs
1
registered plants
2
filings across 1 regulators

Registered plants

Site FDA FEI
Surat, India Not on file

What they file, and where

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 2 None
CDSCO (India) None 2

Questions about Ctx Life Sciences

Does Ctx Life Sciences hold a US DMF or a CEP?
Ctx Life Sciences holds 17 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Ctx Life Sciences manufacture?
1 registered site is on record, in India (Surat). Every site is listed on this page with the register it came from.
What does Ctx Life Sciences make?
16 molecules are on record against Ctx Life Sciences, including Hydrochlorothiazide, Metoprolol, Xylometazoline and Acetazolamide. Each links through to that molecule's full manufacturer list.
Which regulators recognise Ctx Life Sciences's GMP?
Current GMP certificates are on record from CDSCO (India). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • 1 active litigation matter is on record.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates