Suppliers / Deft Organics

Deft Organics

India 46 employees Updated 9 July 2026

Deft Organics is an API manufacturer based in India. It holds one active US drug master file.

1
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
Gwalior, India 3038945565

What they file, and where

Molecule Regulators Docs
Enoxaparin US FDA 1

Also appears on these molecule pages

Enoxaparin API

Questions about Deft Organics

Does Deft Organics hold a US DMF or a CEP?
Deft Organics holds 1 active US drug master file. 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.
Is Deft Organics FDA-registered?
One site operated by Deft Organics carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Deft Organics manufacture?
1 registered site is on record, in India (Gwalior). Every site is listed on this page with the register it came from.
What does Deft Organics make?
1 molecule is on record against Deft Organics, including Enoxaparin. Each links through to that molecule's full manufacturer list.

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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability