Suppliers / Ind Swift

Ind Swift

India 899 employees 2 duplicate records merged Updated 9 July 2026

Ind Swift is a finished-dose manufacturer based in India. It appears in 65 regulatory filings across 9 regulators, without an active US DMF or CEP on file. Its filings concentrate with TMDA (TZ), MINSA (CR) and EFDA (ET). Its GMP standing is certified by NAFDAC (NG) and MHRA (UK). Customs aggregates show $46.3M of exports covering 1,797 molecules to 49 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
65
filings across 9 regulators

Registered plants

Site FDA FEI
Punjab, United Arab Emirates Not on file
DISTRICT S.A.S. NAGAR (MOHALI), India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
TMDA (TZ) 25 None
MINSA (CR) 8 None
EFDA (ET) 7 None
NAFDAC (NG) 7 1
EDE (AE) 5 None
DAV (Vietnam) 4 None
MHRA (UK) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $19K 1
2025 Not reported $46.3M 49
2024 Not reported $45.4M 49
2023 Not reported $41.3M 47

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 We do not publish the identity of any buyer.

Questions about Ind Swift

Does Ind Swift hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Ind Swift. It does have 65 filings with 9 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Ind Swift manufacture?
2 registered sites are on record, in United Arab Emirates and India (Punjab and District S.a.s. Nagar (mohali)). Every site is listed on this page with the register it came from.
Which regulators recognise Ind Swift's GMP?
Current GMP certificates are on record from NAFDAC (NG) and MHRA (UK). 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