Suppliers / Medigraph Pharmaceuticals

Medigraph Pharmaceuticals

India Updated 9 July 2026

Medigraph Pharmaceuticals is an API manufacturer based in India. It holds one valid CEP across a filed portfolio of 3 molecules. Its GMP standing is certified by EMA. Customs aggregates show $6.6M of exports covering 81 molecules to 30 destinations in 2025.

0
active US DMFs
1
valid CEPs
3
registered plants
2
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Taloja, India Not on file
M. 1. 0. C. Taloja, Dist. Raigad, India Not on file
Mumbai, India Not on file

What they file, and where

Molecule Regulators Docs
Bupivacaine EDQM 1
Meperidine SFDA (Saudi Arabia) 1
Olopatadine SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 2 None
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $163K 6
2025 Not reported $6.6M 30
2024 Not reported $703K 29
2023 Not reported $1.4M 29

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 We do not publish the identity of any buyer.

Questions about Medigraph Pharmaceuticals

Does Medigraph Pharmaceuticals hold a US DMF or a CEP?
Medigraph Pharmaceuticals holds 1 valid CEP. 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.
Where does Medigraph Pharmaceuticals manufacture?
3 registered sites are on record, in India (Taloja, M. 1. 0. C. Taloja, Dist. Raigad and Mumbai). Every site is listed on this page with the register it came from.
What does Medigraph Pharmaceuticals make?
3 molecules are on record against Medigraph Pharmaceuticals, including Bupivacaine, Meperidine and Olopatadine. Each links through to that molecule's full manufacturer list.
Which regulators recognise Medigraph Pharmaceuticals's GMP?
Current GMP certificates are on record from EMA. 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
Customs aggregates
Export values, molecule and destination counts