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 We do not publish the identity of any buyer.

Questions about Chemeca Drugs

Does Chemeca Drugs hold a US DMF or a CEP?
Chemeca Drugs holds 12 active US drug master files. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Is Chemeca Drugs FDA-registered?
One site operated by Chemeca Drugs carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Chemeca Drugs's last inspection go?
The most recent inspection on record closed on 3 March 2023 as NAI (No Action Indicated: nothing objectionable was found). 1 inspection is on file.
Where does Chemeca Drugs manufacture?
1 registered site is on record, in India (Anakapalli District). Every site is listed on this page with the register it came from.
What does Chemeca Drugs make?
13 molecules are on record against Chemeca Drugs, including Bupropion, Carisoprodol, Celecoxib and Clopidogrel. Each links through to that molecule's full manufacturer list.

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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Open risk flags

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

Comparable suppliers

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

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