Suppliers / Mylan Laboratories Ltd/India

Mylan Laboratories Ltd/India

India 3 duplicate records merged Updated 9 July 2026

Mylan Laboratories Ltd/India is an API and finished-dose manufacturer based in India. It appears in 18 regulatory filings across 1 regulator, without an active US DMF or CEP on file.

0
active US DMFs
0
valid CEPs
0
registered plants
18
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Ferric Carboxymaltose SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Daclatasvir finished dose Ferric Carboxymaltose API

Filings and GMP by regulator

Regulator Filings GMP certificates
UZPHARM (UZ) 18 None

Questions about Mylan Laboratories Ltd/India

Does Mylan Laboratories Ltd/India hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Mylan Laboratories Ltd/India. It does have 18 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
What does Mylan Laboratories Ltd/India make?
1 molecule is on record against Mylan Laboratories Ltd/India, including Ferric Carboxymaltose. Each links through to that molecule's full manufacturer list.
Where does Mylan Laboratories Ltd/India file?
Filings are on record with UZPHARM (UZ), 18 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