Suppliers / Ciron Drugs & Pharmaceuticals

Ciron Drugs & Pharmaceuticals

India 753 employees Updated 9 July 2026

Ciron Drugs & Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 212 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), ARCSA (EC) and ZAMRA (ZM). Its GMP standing is certified by FDA (GH), NAFDAC (NG) and ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
4
registered plants 1 with an FDA FEI number
212
filings across 8 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
TARAPUR, India Not on file
Tarapur, India 3017545500
Palghar, Nigeria Not on file
Maharashtra State India, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 89 2
ARCSA (EC) 45 None
ZAMRA (ZM) 22 None
DIGEMAPS (DO) 21 None
FDA (GH) 20 2
MINSA (CR) 13 None
ANVISA (Brazil) None 2

Questions about Ciron Drugs & Pharmaceuticals

Does Ciron Drugs & Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Ciron Drugs & Pharmaceuticals. It does have 212 filings with 8 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Ciron Drugs & Pharmaceuticals FDA-registered?
One site operated by Ciron Drugs & Pharmaceuticals 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 Ciron Drugs & Pharmaceuticals manufacture?
4 registered sites are on record, in India and Nigeria (Tarapur, Tarapur and Palghar among others). Every site is listed on this page with the register it came from.
Which regulators recognise Ciron Drugs & Pharmaceuticals's GMP?
Current GMP certificates are on record from FDA (GH), NAFDAC (NG) and ANVISA (Brazil). 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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Sources on this page

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