Drug company (FDA labeler)
Verityrx, LLC
Name in FDA records: VERITYRX, LLC
NDC labeler code: 83939
What is a labeler?
The company whose name is on the package and in the FDA’s National Drug Code (NDC) Directory. It may make the medicine itself or sell medicine made by another company. The first part of every NDC code identifies the labeler.
Official FDA data only
Products, approvals and recalls come from the FDA (NDC Directory, Drugs@FDA, enforcement reports). Recalls are linked to this company by the NDC labeler code on the recalled product.
Questions about your medicine: ask your doctor or pharmacist. In an emergency, call 911.
Prescription medicines
- ClonidineClonidine Transdermal System, Catapres-Tts-1, Clonidine Transdermal System Usp, 0.1 Mg/Day · 2 products
- CiprofloxacinCiprofloxacin in Dextrose, Cipro, Ciloxan · 1 product
- Nitrofurantoin1 product
- ClindamycinCleocin Phosphate, Cleocin Hydrochloride, Clindamycin Phoaphate Topical Solution Usp, 1% · 1 product
- Levofloxacin1 product
- OxybutyninOxytrol · 1 product
- Sulfamethoxazole and trimethoprimSulfamethoxazole and Trimethoprim Ds, Sulfatrim, Bactrim Ds · 1 product
FDA applications for these products
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| March 21, 2023 | ANDA217272 | Nitrofurantoin NITROFURANTOIN | Mankind Pharma |
| October 23, 2017 | ANDA209823 | Oxybutynin OXYBUTYNIN CHLORIDE | Novitium Pharma |
| January 8, 2015 | ANDA202801 | Levofloxacin LEVOFLOXACIN | Hetero Labs Ltd V |
| December 6, 2011 | ANDA091368 | Clonidine CLONIDINE HYDROCHLORIDE | Alembic Pharms Ltd |
| February 16, 2010 | ANDA090624 | Sulfamethoxazole and trimethoprim SULFAMETHOXAZOLE AND TRIMETHOPRIM | Aurobindo Pharma |
| August 26, 2009 | ANDA065442 | Clindamycin CLINDAMYCIN HYDROCHLORIDE | Aurobindo Pharma |
| August 26, 2009 | ANDA078895 | Clonidine CLONIDINE HYDROCHLORIDE | Unichem |
| March 16, 2004 | ANDA076593 | Ciprofloxacin CIPROFLOXACIN, CIPROFLOXACIN HYDROCHLORIDE | Aiping Pharm Inc |
The sponsor is the company that holds the FDA application; it can differ from the labeler.
Recall timeline
No recall of these products (by NDC code) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026