Suppliers / Tagoor Laboratories

Tagoor Laboratories

India 247 employees Updated 9 July 2026

Tagoor Laboratories is an API manufacturer based in India. It holds 4 valid CEPs across a filed portfolio of 4 molecules. Customs aggregates show $6.9M of exports covering 218 molecules to 31 destinations in 2025.

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

Registered plants

Site FDA FEI
Visakhapatnam, India 3025582980
West Godavari, India 3016446284
East Godavari, India 3030640551

What they file, and where

Molecule Regulators Docs
Lipoic Acid EDQM 1
Loratadine EDQM 1
Pantoprazole EDQM 1
Rupatadine EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 2 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $3.0M 16
2025 Not reported $6.9M 31
2024 Not reported $11.0M 30
2023 Not reported $6.4M 24

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 We do not publish the identity of any buyer.

Questions about Tagoor Laboratories

Does Tagoor Laboratories hold a US DMF or a CEP?
Tagoor Laboratories holds 4 valid CEPs. 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 Tagoor Laboratories FDA-registered?
3 sites operated by Tagoor Laboratories carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Tagoor Laboratories manufacture?
3 registered sites are on record, in India (Visakhapatnam, West Godavari and East Godavari). Every site is listed on this page with the register it came from.
What does Tagoor Laboratories make?
4 molecules are on record against Tagoor Laboratories, including Lipoic Acid, Loratadine, Pantoprazole and Rupatadine. Each links through to that molecule's full manufacturer list.
Where does Tagoor Laboratories file?
Filings are on record with CDSCO (India), 2 in total.

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
Customs aggregates
Export values, molecule and destination counts