Suppliers / Chemeca Drugs

Chemeca Drugs

India 60 employees Updated 9 July 2026

Chemeca Drugs is an API manufacturer based in India. It holds 12 active US drug master files across a filed portfolio of 13 molecules. Its most recent recorded inspection, by US FDA, closed on 3 March 2023 as NAI. Customs aggregates show $11.8M of exports covering 98 molecules to 8 destinations in 2025.

12
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 3 March 2023 NAI US FDA

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

Registered plants

Site FDA FEI
Anakapalli District, India 3010630993

What they file, and where

Molecule Regulators Docs
Bupropion US FDA 1
Carisoprodol US FDA 1
Celecoxib US FDA 1
Clopidogrel US FDA 1
Clopidogrel Bisulfate SFDA (Saudi Arabia) 1
Diltiazem US FDA 1
Fexofenadine US FDA 1
Fluoxetine US FDA 1
Hydralazine US FDA 1
Pirfenidone US FDA 1
Show all 13 molecules on file
Quetiapine US FDA 1
Rifaximin US FDA 1
Sertraline US FDA 1

Also appears on these molecule pages

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $3.1M 2
2025 Not reported $11.8M 8
2024 Not reported $13.0M 8
2023 Not reported $6.1M 8

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 We do not publish the identity of any buyer.

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Open risk flags

  • The most recent inspection outcome was NAI, on 3 March 2023.

Sources on this page

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