Suppliers / Rl Fine Chem

Rl Fine Chem

India Updated 9 July 2026

The public registers hold a second record for Rl Fine Chem. The fuller profile, with 27 active US DMFs and 0 valid CEPs, is at R.L. Fine Chem. Figures on this page cover only this record.

Rl Fine Chem is an API manufacturer based in India. It holds 13 active US drug master files across a filed portfolio of 14 molecules.

13
active US DMFs
0
valid CEPs
0
registered plants
2
filings across 1 regulators

What they file, and where

Molecule Regulators Docs
Alprazolam US FDA 1
Amitriptyline US FDA 1
Chlorpromazine US FDA 1
Clomipramine US FDA 1
Cyclobenzaprine US FDA 1
Doxylamine US FDA 1
Duloxetine US FDA 1
Imipramine US FDA 1
Lorazepam US FDA 1
Meclizine US FDA 1
Show all 14 molecules on file
Nortriptyline US FDA 1
Orphenandrine Citrate SFDA (Saudi Arabia) 1
Oxazepam US FDA 1
Sertraline US FDA 1

Also appears on these molecule pages

Alprazolam API Amitriptyline API Chlorpromazine API Clomipramine API Cyclobenzaprine API Doxylamine API Lorazepam API Nortriptyline API Oxazepam API Sertraline API Duloxetine API Meclizine API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 2 None

Questions about Rl Fine Chem

Does Rl Fine Chem hold a US DMF or a CEP?
Rl Fine Chem holds 13 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.
What does Rl Fine Chem make?
14 molecules are on record against Rl Fine Chem, including Alprazolam, Amitriptyline, Chlorpromazine and Clomipramine. Each links through to that molecule's full manufacturer list.
Where does Rl Fine Chem file?
Filings are on record with MINSA (CR), 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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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