Suppliers / Anthea Pharma

Anthea Pharma

India 453 employees Updated 9 July 2026

Anthea Pharma is a finished-dose manufacturer based in India. It appears in 12 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Customs aggregates show $1.2M of exports covering 27 molecules to 4 destinations in 2025.

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

Registered plants

Site FDA FEI
Sangareddy, India 3026048557

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA 12 None

Scale

Year Revenue Exports Destinations
2025 Not reported $1.2M 4

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 We do not publish the identity of any buyer.

Questions about Anthea Pharma

Does Anthea Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Anthea Pharma. It does have 12 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is Anthea Pharma FDA-registered?
One site operated by Anthea Pharma 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.
Where does Anthea Pharma manufacture?
1 registered site is on record, in India (Sangareddy). Every site is listed on this page with the register it came from.
Where does Anthea Pharma file?
Filings are on record with US FDA, 12 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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Comparable suppliers

Abbott Healthcare also in India Accent Pharmaceuticals Diagnostics also in India Accure Labs Pvt.Ltd also in India ACME Formulation also in India Acme Generics also in India

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