Register entry
- Registered sites
- 0
- Active NDC listings
- 27
- Labeller names
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
2727 active NDC listings: 27 human prescription drug. By marketing category: NDA 27.
| Dosage form | NDCs |
|---|---|
| tablet | 15 |
| tablet, sugar coated | 6 |
| capsule, extended release | 3 |
| solution | 3 |
| Route | NDCs |
|---|---|
| oral | 27 |
| Labeller name on the listing | NDCs |
|---|---|
| validus pharmaceuticals llc | 25 |
| validus pharmaceuticals llc | 2 |
Catalogue
Marketed products
27| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| ATONCY | Atomoxetine hydrochloride | solution, oral | 30698-456NDA |
| Bumex | Bumetanide | tablet, oral | 30698-630NDA |
| Bumex | Bumetanide | tablet, oral | 30698-631NDA |
| Bumex | Bumetanide | tablet, oral | 30698-632NDA |
| EQUETRO | Carbamazepine | capsule, extended release, oral | 30698-419NDA |
| EQUETRO | Carbamazepine | capsule, extended release, oral | 30698-421NDA |
| EQUETRO | Carbamazepine | capsule, extended release, oral | 30698-423NDA |
| LOPRESSOR | METOPROLOL TARTRATE | tablet, oral | 30698-460NDA |
| LOPRESSOR | Metoprolol Tartrate | solution, oral | 30698-464NDA |
| Lasix | FUROSEMIDE | tablet, oral | 30698-060NDA |
| Lasix | FUROSEMIDE | tablet, oral | 30698-066NDA |
| Lasix | FUROSEMIDE | tablet, oral | 30698-067NDA |
| Lopressor | metoprolol tartrate | tablet, oral | 30698-458NDA |
| Lopressor | metoprolol tartrate | tablet, oral | 30698-459NDA |
| Lotensin | benazepril hydrochloride | tablet, oral | 30698-448NDA |
| Lotensin | benazepril hydrochloride | tablet, oral | 30698-449NDA |
| Lotensin | benazepril hydrochloride | tablet, oral | 30698-450NDA |
| Lotensin HCT | benazepril hydrochloride and hydrochlorothiazide | tablet, oral | 30698-452NDA |
| Lotensin HCT | benazepril hydrochloride and hydrochlorothiazide | tablet, oral | 30698-453NDA |
| Lotensin HCT | benazepril hydrochloride and hydrochlorothiazide | tablet, oral | 30698-454NDA |
| Norpramin | desipramine hydrochloride | tablet, sugar coated, oral | 30698-007NDA |
| Norpramin | desipramine hydrochloride | tablet, sugar coated, oral | 30698-011NDA |
| Norpramin | desipramine hydrochloride | tablet, sugar coated, oral | 30698-015NDA |
| Norpramin | desipramine hydrochloride | tablet, sugar coated, oral | 30698-019NDA |
| Norpramin | desipramine hydrochloride | tablet, sugar coated, oral | 30698-020NDA |
| Norpramin | desipramine hydrochloride | tablet, sugar coated, oral | 30698-021NDA |
| RALDESY TM | TRAZODONE HYDROCHLORIDE ORAL | solution, oral | 30698-455NDA |
Compare
Other companies listing desipramine hydrochloride
- RemedyRepack, Inc1 site · 1,521 NDC
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.1 site · 273 NDC
- Ingenus Pharmaceuticals, LLC0 sites · 142 NDC
Enquiry
Common questions
- Is Validus Pharmaceuticals LLC FDA approved?
- Validus Pharmaceuticals LLC holds no registered establishment of its own; 27 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Validus Pharmaceuticals LLC make?
- 27 products are listed under Validus Pharmaceuticals LLC in the openFDA NDC Directory, most often as tablet; tablet, sugar coated; capsule, extended release. The full breakdown by dosage form and route is above. A listing count is not a sales figure.
Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.