Suppliers / Inject Care Parenterals

Inject Care Parenterals

India Updated 9 July 2026

Inject Care Parenterals is a finished-dose manufacturer based in India. It appears in 37 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG), EFDA (ET) and ARCSA (EC). Its GMP standing is certified by CDSCO (India), EMA and TMDA (TZ). Customs aggregates show $12.2M of exports covering 222 molecules to 21 destinations in 2025.

0
active US DMFs
0
valid CEPs
5
registered plants
37
filings across 4 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
Vapi, India Not on file
vapi vapi 396 195 valsad, India Not on file
Vapi, India Not on file
vapivapi 396 195 valsad, India Not on file
Gujarat, Tanzania Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 27 None
EFDA (ET) 5 None
ARCSA (EC) 4 None
TMDA (TZ) 1 1
CDSCO (India) None 3
EMA None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $2.0M 8
2025 Not reported $12.2M 21
2024 Not reported $7.0M 16
2023 Not reported $8.2M 15

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 We do not publish the identity of any buyer.

Questions about Inject Care Parenterals

Does Inject Care Parenterals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Inject Care Parenterals. It does have 37 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Inject Care Parenterals manufacture?
5 registered sites are on record, in India and Tanzania (Vapi, Vapi Vapi 396 195 Valsad and Vapivapi 396 195 Valsad among others). Every site is listed on this page with the register it came from.
Which regulators recognise Inject Care Parenterals's GMP?
Current GMP certificates are on record from CDSCO (India), EMA and TMDA (TZ). 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