Suppliers / Veranova Lp

Veranova Lp

United States Updated 9 July 2026

Veranova Lp is an API manufacturer based in United States. It holds 49 active US drug master files.

49
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Dextroamphetamine US FDA 4
Amphetamine US FDA 3
Methylphenidate US FDA 3
Oxycodone US FDA 3
Dronabinol US FDA 2
Fentanyl US FDA 2
Alfentanil US FDA 1
Auranofin US FDA 1
Benzhydrocodone US FDA 1
Cangrelor US FDA 1
Show all 30 molecules on file
Cannabidiol US FDA 1
Carboplatin US FDA 1
Cisplatin US FDA 1
Clevidipine US FDA 1
Codeine US FDA 1
Dantrolene US FDA 1
Decitabine US FDA 1
Dexmethylphenidate US FDA 1
Difenoxin US FDA 1
Diphenoxylate US FDA 1
Edrophonium US FDA 1
Fluvoxamine US FDA 1
Hydrocodone US FDA 1
Hydromorphone US FDA 1
Lenalidomide US FDA 1
Lurasidone US FDA 1
Metamfetamine US FDA 1
Morphine US FDA 1
Nintedanib US FDA 1
Oxaliplatin US FDA 1

Also appears on these molecule pages

Show 14 more molecule pages

Questions about Veranova Lp

Does Veranova Lp hold a US DMF or a CEP?
Veranova Lp holds 49 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 Veranova Lp make?
30 molecules are on record against Veranova Lp, including Dextroamphetamine, Amphetamine, Methylphenidate and Oxycodone. Each links through to that molecule's full manufacturer list.

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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Open risk flags

  • 2 active litigation matters are on record.

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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability