Suppliers / Endoc Biotech

Endoc Biotech

India Updated 9 July 2026

Endoc Biotech 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
Rajkot, India 3042715330

What they file, and where

Molecule Regulators Docs
Mupirocin US FDA 1

Also appears on these molecule pages

Mupirocin API

Questions about Endoc Biotech

Does Endoc Biotech hold a US DMF or a CEP?
Endoc Biotech 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 Endoc Biotech FDA-registered?
One site operated by Endoc Biotech 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 Endoc Biotech manufacture?
1 registered site is on record, in India (Rajkot). Every site is listed on this page with the register it came from.
What does Endoc Biotech make?
1 molecule is on record against Endoc Biotech, including Mupirocin. 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