Suppliers / Shaimil Laboratories

Shaimil Laboratories

India 36 employees 2 duplicate records merged Updated 9 July 2026

Shaimil Laboratories is a finished-dose manufacturer based in India. It appears in 7 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by CDSCO (India). Customs aggregates show $634K of exports covering 127 molecules to 6 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
7
filings across 1 regulators

Registered plants

Site FDA FEI
makarpura vadodara 390 010 vadodara, India Not on file
G.I.D.C., India Not on file
makarpurava dodara 390 010vadodara, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 7 None
CDSCO (India) None 3

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $253K 3
2025 Not reported $634K 6
2024 Not reported $1.2M 7
2023 Not reported $453K 6

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 We do not publish the identity of any buyer.

Questions about Shaimil Laboratories

Does Shaimil Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Shaimil Laboratories. It does have 7 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Shaimil Laboratories manufacture?
3 registered sites are on record, in India (Makarpura Vadodara 390 010 Vadodara, G.i.d.c. and Makarpurava Dodara 390 010vadodara). Every site is listed on this page with the register it came from.
Which regulators recognise Shaimil Laboratories's GMP?
Current GMP certificates are on record from CDSCO (India). 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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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
Customs aggregates
Export values, molecule and destination counts