Drug company (FDA labeler)
Validus Pharmaceuticals LLC
NDC labeler code: 30698
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
- Desipramine hydrochlorideNorpramin · 6 products
- MetoprololToprol XL, Lopressor, Kapspargo · 4 products
- CarbamazepineTegretol XR, Equetro, Carbatrol · 3 products
- Benazepril hydrochlorideLotensin · 3 products
- BumetanideBumex, Enbumyst · 3 products
- FurosemideLasix, Furoscix, Lasix Onyu · 3 products
- Benazepril hydrochloride and hydrochlorothiazideLotensin Hct · 3 products
- AtomoxetineStrattera, Atoncy · 1 product
- Trazodone hydrochlorideRaldesy Tm · 1 product
- PentoxifyllineTrental · 1 product
FDA applications for these products
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Approved | Application | Medicine | Sponsor |
|---|---|---|---|
| March 20, 2026 | NDA220320 | Atomoxetine ATONCY | MAP77 |
| August 28, 2025 | NDA218698 | Metoprolol LOPRESSOR | Xtm Consulting |
| April 10, 2025 | NDA219373 | Metoprolol LOPRESSOR | Rubicon Research |
| November 26, 2024 | NDA218637 | Trazodone hydrochloride RALDESY | Kamat |
| December 10, 2004 | NDA021710 | Carbamazepine EQUETRO | Validus Pharms |
| May 19, 1992 | NDA020033 | Benazepril hydrochloride and hydrochlorothiazide LOTENSIN HCT | Validus Pharms |
| June 25, 1991 | NDA019851 | Benazepril hydrochloride LOTENSIN | Validus Pharms |
| August 30, 1984 | NDA018631 | Pentoxifylline TRENTAL | Validus Pharms |
| February 28, 1983 | NDA018225 | Bumetanide BUMEX | Validus Pharms |
| August 7, 1978 | NDA017963 | Metoprolol LOPRESSOR | Validus Pharms |
| July 1, 1966 | NDA016273 | Furosemide LASIX | Validus Pharms |
| November 20, 1964 | NDA014399 | Desipramine hydrochloride NORPRAMIN | Validus Pharms |
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