Suppliers / Recipharm pharmaservices

Recipharm pharmaservices

India Updated 9 July 2026

Recipharm pharmaservices is a finished-dose manufacturer based in India. It appears in 3 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with BOMRA (BW), NAFDAC (NG) and NPRA (MY). Its GMP standing is certified by EMA, CDSCO (India) and MFDS (Korea), among 5 authorities. Its most recent recorded inspection, by US FDA, closed on 22 March 2024 as NAI. Customs aggregates show $11.0M of exports covering 587 molecules to 14 destinations in 2025.

0
active US DMFs
0
valid CEPs
4
registered plants 1 with an FDA FEI number
3
filings across 3 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
6 of 6 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 22 March 2024 NAI US FDA
  • 13 February 2020 VAI US FDA
  • 1 February 2019 VAI US FDA
  • 11 May 2018 NAI US FDA
  • 19 March 2015 NAI US FDA
  • 1 November 2012 VAI US FDA

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

Registered plants

Site FDA FEI
Bengaluru, India 3009150119
NELAMANGALA, India Not on file
Bengaluru, India Not on file
bengaluru 562 123, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
BOMRA (BW) 1 None
NAFDAC (NG) 1 None
NPRA (MY) 1 None
EMA None 4
CDSCO (India) None 3
MFDS (Korea) None 2
US FDA None 1
ANVISA (Brazil) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $2.4M 10
2025 Not reported $11.0M 14
2024 Not reported $7.3M 17
2023 Not reported $9.0M 15

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Recipharm pharmaservices

Does Recipharm pharmaservices hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Recipharm pharmaservices. It does have 3 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Recipharm pharmaservices FDA-registered?
One site operated by Recipharm pharmaservices 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 Recipharm pharmaservices's last inspection go?
The most recent inspection on record closed on 22 March 2024 as NAI (No Action Indicated: nothing objectionable was found). 6 inspections are on file.
Where does Recipharm pharmaservices manufacture?
4 registered sites are on record, in India (Bengaluru, Nelamangala and Bengaluru 562 123 among others). Every site is listed on this page with the register it came from.
Which regulators recognise Recipharm pharmaservices's GMP?
Current GMP certificates are on record from EMA, CDSCO (India), MFDS (Korea), US FDA 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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Open risk flags

  • The most recent inspection outcome was NAI, on 22 March 2024.

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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
Customs aggregates
Export values, molecule and destination counts