Suppliers / Zenara

Zenara

India 182 employees Updated 9 July 2026

Zenara is a finished-dose manufacturer based in India. It appears in 24 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with US FDA, CDSCO (India) and MINSA (CR). Its GMP standing is certified by MHRA (UK) and US FDA. Its most recent recorded inspection, by US FDA, closed on 21 May 2024 as VAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
24
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 21 May 2024 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Hyderabad, India 3005485158

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 18 1
CDSCO (India) 5 None
MINSA (CR) 1 None
MHRA (UK) None 1

Questions about Zenara

Does Zenara hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Zenara. It does have 24 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Zenara FDA-registered?
One site operated by Zenara 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.
How did Zenara's last inspection go?
The most recent inspection on record closed on 21 May 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Zenara manufacture?
1 registered site is on record, in India (Hyderabad). Every site is listed on this page with the register it came from.
Which regulators recognise Zenara's GMP?
Current GMP certificates are on record from MHRA (UK) and US FDA. 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

  • 24 active litigation matters are on record.
  • The most recent inspection outcome was VAI, on 21 May 2024.

Comparable suppliers

Abbott Healthcare also in India Accent Pharmaceuticals Diagnostics also in India Accure Labs Pvt.Ltd also in India ACME Formulation also in India Acme Generics also in India

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
EudraGMDP and national regulators
GMP certificates