Suppliers / Hab Pharmaceuticals & Research

Hab Pharmaceuticals & Research

India Updated 9 July 2026

Hab Pharmaceuticals & Research is a finished-dose manufacturer based in India. It appears in 35 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by TMDA (TZ) and NAFDAC (NG). Customs aggregates show $22.0M of exports covering 762 molecules to 16 destinations in 2025.

0
active US DMFs
0
valid CEPs
1
registered plants
35
filings across 1 regulators

Registered plants

Site FDA FEI
DEHRADUN, Tanzania Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
NAFDAC (NG) 35 1
TMDA (TZ) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $2.1M 6
2025 Not reported $22.0M 16
2024 Not reported $10.8M 14
2023 Not reported $11.3M 15

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 We do not publish the identity of any buyer.

Questions about Hab Pharmaceuticals & Research

Does Hab Pharmaceuticals & Research hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Hab Pharmaceuticals & Research. It does have 35 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Hab Pharmaceuticals & Research manufacture?
1 registered site is on record, in Tanzania (Dehradun). Every site is listed on this page with the register it came from.
Which regulators recognise Hab Pharmaceuticals & Research's GMP?
Current GMP certificates are on record from TMDA (TZ) and NAFDAC (NG). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts