Suppliers / Pure And Cure Healthcare

Pure And Cure Healthcare

India Updated 9 July 2026

Pure And Cure Healthcare is an API and finished-dose manufacturer based in India. It holds 19 active US drug master files across a filed portfolio of 11 molecules. Its filings concentrate with CDSCO (India) and FDA (GH). Its most recent recorded inspection, by US FDA, closed on 25 September 2015 as VAI. Customs aggregates show $2.8M of exports covering 134 molecules to 14 destinations in 2025.

19
active US DMFs
0
valid CEPs
3
registered plants 3 with an FDA FEI number
95
filings across 2 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
3 of 3 confirmed
Inspections
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 25 September 2015 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
India, India 3007577941
Panchkula, India 3024206690
India, India 3008176882

What they file, and where

Molecule Regulators Docs
Cefuroxime US FDA 9
Bosentan US FDA 1
Cefalotin US FDA 1
Cefixime US FDA 1
Cefpodoxime US FDA 1
Cefprozil US FDA 1
Ceftazidime US FDA 1
Ceftizoxime US FDA 1
Deferasirox US FDA 1
Oxacillin US FDA 1
Show all 11 molecules on file
Pentosan Polysulfate Sodium US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 94 None
FDA (GH) 1 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $377K 4
2025 Not reported $2.8M 14
2024 Not reported $2.8M 15

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 We do not publish the identity of any buyer.

Comparing suppliers?

Choose your molecules and target markets. Pure And Cure Healthcare comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Open risk flags

  • The most recent inspection outcome was VAI, on 25 September 2015.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
Customs aggregates
Export values, molecule and destination counts