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Data / Drug companies / V2 Pharma, LLC

V2 Pharma, LLC: 24 products in the FDA NDC directory, labeler code 72835

V2 Pharma, LLC (labeler code 72835) lists 24 products in the FDA National Drug Code Directory, covering 10 finished drugs by generic name. By type: 15 prescription drugs, 9 over the counter drugs. Its main marketing category is other unapproved drugs. The newest product started marketing on October 28, 2026.

SpecStream is the live web data engine for teams and agents. It reads the National Drug Code Directory that FDA publishes, and this page is that reading. Ask for the companies that make a drug, a class or a dosage form, with their headquarters, website and size added from the web, and new listings and discontinued products arrive in your sheet, CRM, Slack or agent as FDA posts them.

Labeler code
72835
Products in commercial distribution
24
Packages
23
Finished drugs by generic name
10
Prescription products
15
Over the counter products
9
Flagged as original packager
22 of 22 products that carry the flag
Started marketing in the last 12 months
9
Earliest marketing start
June 3, 2019
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Other unapproved drugs1562.5%
Over the counter monograph drugs833.3%
Generic drugs (ANDA)14.2%

Products by type

TypeProductsShare
Prescription drugs1562.5%
Over the counter drugs937.5%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

DrugProductsCompanies listing it
Lidocaine4216
Lidocaine 4%445
Diclofenac sodium and menthol, methyl salicylate42
Lidocaine hydrochloride3134
Calcipotriene cream, 0.005% and transparent dressing21
Capsaicin166
Leflunomide and diclofenac sodium gel11
Diclofenac sodium and menthol / camphor gel11
Triamcinolone acetonide cream 0.1%, transparent dressing11
Methyl salicylate, menthol115

Dosage forms

Dosage formProductsShare
Kit1354.2%
Cream312.5%
Capsule28.3%
Liquid28.3%
Patch28.3%
Tape14.2%
Gel14.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Lidocaine 4% Patch72835-400PatchOver the counter monograph drugsOctober 28, 2026
Lidoflect72835-404PatchOver the counter monograph drugsOctober 20, 2026
Lidovyx72835-447GelOver the counter monograph drugsJune 25, 2026
Lidozall Pro72835-445CreamOver the counter monograph drugsJune 16, 2026
Dermavyx72835-777KitOther unapproved drugsMay 5, 2026
Orthrexo72835-333KitOther unapproved drugsApril 2, 2026
LidoTape72835-040TapeOver the counter monograph drugsApril 1, 2026
Relivyx Plus72835-555KitOther unapproved drugsMarch 31, 2026
Cipotrex72835-922KitOther unapproved drugsMarch 27, 2026
Crysalo72835-511LiquidOther unapproved drugsAugust 21, 2025
Orthaphen72835-222KitOther unapproved drugsJuly 28, 2025
Syntherma Plus72835-105KitOther unapproved drugsJuly 1, 2025
Matervia72835-660CapsuleOther unapproved drugsJune 11, 2025
Cobalefol72835-550CapsuleOther unapproved drugsMay 16, 2025
Zestama72835-175LiquidOver the counter monograph drugsApril 1, 2025
Lidozall Plus72835-114CreamOver the counter monograph drugsFebruary 11, 2025
Lidozall72835-004CreamOver the counter monograph drugsNovember 21, 2024
Inflatherm72835-701KitOther unapproved drugsAugust 13, 2024
Trionex72835-902KitOther unapproved drugsJanuary 13, 2023
Lefluniclo72835-602KitOther unapproved drugsJanuary 11, 2023
Elemar Patch72835-502KitOther unapproved drugsFebruary 22, 2022
Fenovar72835-202KitOther unapproved drugsJanuary 21, 2022
LMR Plus72835-501KitOther unapproved drugsJune 3, 2019
Varophen72835-201KitGeneric drugs (ANDA)June 3, 2019

Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.