Suppliers / Makcur Laboratories

Makcur Laboratories

India 2 duplicate records merged Updated 9 July 2026

Makcur Laboratories is a finished-dose manufacturer based in India. It appears in 96 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), NAFDAC (NG) and ARCSA (EC). Its GMP standing is certified by CDSCO (India), FDA (GH) and NAFDAC (NG). Customs aggregates show $4.6M of exports covering 307 molecules to 27 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
96
filings across 7 regulators

Registered plants

Site FDA FEI
Village, India Not on file
tal dehgam zak gandhinagar, India Not on file
tal dehgamzakgandhin agar, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 38 None
NAFDAC (NG) 24 1
ARCSA (EC) 21 None
UZPHARM (UZ) 5 None
EFDA (ET) 4 None
MINSA (CR) 2 None
CDSCO (India) None 3
FDA (GH) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $440K 9
2025 Not reported $4.6M 27
2024 Not reported $5.7M 22
2023 Not reported $4.6M 21

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 We do not publish the identity of any buyer.

Questions about Makcur Laboratories

Does Makcur Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Makcur Laboratories. It does have 96 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Makcur Laboratories manufacture?
3 registered sites are on record, in India (Village, Tal Dehgam Zak Gandhinagar and Tal Dehgamzakgandhin Agar). Every site is listed on this page with the register it came from.
Which regulators recognise Makcur Laboratories's GMP?
Current GMP certificates are on record from CDSCO (India), FDA (GH) and NAFDAC (NG). 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