Suppliers / Caplin Point Laboratories

Caplin Point Laboratories

India Updated 9 July 2026

Caplin Point Laboratories is a finished-dose manufacturer based in India. It appears in 1,112 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), ARCSA (EC) and MINSA (CR). Customs aggregates show $87.3M of exports covering 3,445 molecules to 21 destinations in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
1,112
filings across 5 regulators

Registered plants

Site FDA FEI
CHENNAI, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 721 None
ARCSA (EC) 292 None
MINSA (CR) 88 None
INVIMA (CO) 10 None
COFEPRIS (MX) 1 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $12.6M 11
2025 Not reported $87.3M 21
2024 Not reported $87.4M 19
2023 Not reported $91.3M 19

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 We do not publish the identity of any buyer.

Questions about Caplin Point Laboratories

Does Caplin Point Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Caplin Point Laboratories. It does have 1,112 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Caplin Point Laboratories manufacture?
1 registered site is on record, in India (Chennai). Every site is listed on this page with the register it came from.
Where does Caplin Point Laboratories file?
Filings are on record with DIGEMAPS (DO), ARCSA (EC), MINSA (CR), INVIMA (CO) and 1 other regulator, 1,112 in total.

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
Customs aggregates
Export values, molecule and destination counts