Suppliers / Antila Lifesciences

Antila Lifesciences

India 58 employees 2 duplicate records merged Updated 9 July 2026

Antila Lifesciences is a finished-dose manufacturer based in India. It appears in 49 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), NAFDAC (NG) and DIGEMAPS (DO). Its GMP standing is certified by CDSCO (India). Customs aggregates show $9.4M of exports covering 426 molecules to 17 destinations in 2025.

0
active US DMFs
0
valid CEPs
12
registered plants
49
filings across 6 regulators

Registered plants

Site FDA FEI
tal kalolsantejgandhin agar, India Not on file
Sabarkantha, India Not on file
jarodvadoda ra, India Not on file
ahmedabad, India Not on file
kerala bavla kerala bavla ahmedabad, India Not on file
sanand 382 110 ahmedabad, India Not on file

6 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 32 None
NAFDAC (NG) 7 None
DIGEMAPS (DO) 4 None
FDA (GH) 3 None
MINSA (CR) 2 None
BOMRA (BW) 1 None
CDSCO (India) None 15

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $1.9M 9
2025 Not reported $9.4M 17
2024 Not reported $7.3M 20
2023 Not reported $5.9M 14

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 We do not publish the identity of any buyer.

Questions about Antila Lifesciences

Does Antila Lifesciences hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Antila Lifesciences. It does have 49 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Antila Lifesciences manufacture?
12 registered sites are on record, in India (Tal Kalolsantejgandhin Agar, Sabarkantha and Jarodvadoda Ra among others). Every site is listed on this page with the register it came from.
Which regulators recognise Antila Lifesciences'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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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