Suppliers / Swiss Parenterals

Swiss Parenterals

India 448 employees 5 duplicate records merged Updated 9 July 2026

Swiss Parenterals is a finished-dose manufacturer based in India. It appears in 219 regulatory filings across 17 regulators, without an active US DMF or CEP on file. Its filings concentrate with UZPHARM (UZ), NAFDAC (NG) and TMDA (TZ). Its GMP standing is certified by CDSCO (India), FDA (GH) and EMA, among 6 authorities. Customs aggregates show $32.3M of exports covering 1,317 molecules to 80 destinations in 2025.

0
active US DMFs
0
valid CEPs
12
registered plants
219
filings across 17 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Ahmedabad, United Arab Emirates Not on file
AHMEDABAD, India Not on file
412- 414, India Not on file
bavla 382 220 ahmedabad, India Not on file
nr bavla ahmedabad 382 220 ahmedabad, India Not on file
Ahmedabad, India Not on file

6 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 40 2
NAFDAC (NG) 34 1
TMDA (TZ) 29 None
MINSA (CR) 25 None
ARCSA (EC) 17 None
DIGEMAPS (DO) 15 None
CDSCO (India) None 17
FDA (GH) None 2
EMA None 2
ANVISA (Brazil) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $4.1M 39
2025 Not reported $32.3M 80
2024 Not reported $31.2M 76
2023 Not reported $26.5M 67

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 We do not publish the identity of any buyer.

Questions about Swiss Parenterals

Does Swiss Parenterals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Swiss Parenterals. It does have 219 filings with 17 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Swiss Parenterals manufacture?
12 registered sites are on record, in United Arab Emirates and India (Ahmedabad, Ahmedabad and 412- 414 among others). Every site is listed on this page with the register it came from.
Which regulators recognise Swiss Parenterals's GMP?
Current GMP certificates are on record from CDSCO (India), FDA (GH), EMA, UZPHARM (UZ), ANVISA (Brazil) and 1 more. 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