Suppliers / Vapi Care Pharma

Vapi Care Pharma

India 6 employees 2 duplicate records merged Updated 9 July 2026

Vapi Care Pharma is a finished-dose manufacturer based in India. It appears in 44 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with NAFDAC (NG) and EDE (AE). Its GMP standing is certified by CDSCO (India) and NAFDAC (NG). Customs aggregates show $349K of exports covering 36 molecules to 5 destinations in 2025.

0
active US DMFs
0
valid CEPs
5
registered plants
44
filings across 2 regulators

Registered plants

Site FDA FEI
Gujarat, United Arab Emirates Not on file
Vapi, India Not on file
vapi 396 195 valsad, India Not on file
valsad, India Not on file
Gujarat State, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 43 1
EDE (AE) 1 None
CDSCO (India) None 3

Scale

Year Revenue Exports Destinations
2025 Not reported $349K 5
2024 Not reported $361K 7
2023 Not reported $437K 7
2022 Not reported $315K 5

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 We do not publish the identity of any buyer.

Questions about Vapi Care Pharma

Does Vapi Care Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Vapi Care Pharma. It does have 44 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Vapi Care Pharma manufacture?
5 registered sites are on record, in United Arab Emirates, India and Nigeria (Gujarat, Vapi and Vapi 396 195 Valsad among others). Every site is listed on this page with the register it came from.
Which regulators recognise Vapi Care Pharma's GMP?
Current GMP certificates are on record from CDSCO (India) 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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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