Register entry
- Registered sites
- 0
- Active NDC listings
- 48
- Labeller names
- 3
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
4848 active NDC listings: 48 human prescription drug. By marketing category: ANDA 21, NDA AUTHORIZED GENERIC 15, NDA 12.
| Dosage form | NDCs |
|---|---|
| tablet | 11 |
| tablet, film coated | 7 |
| capsule, delayed release | 4 |
| kit | 4 |
| capsule, extended release | 3 |
| capsule, gelatin coated | 3 |
| injection | 3 |
| suspension | 3 |
| tablet, delayed release | 3 |
| granule, for suspension | 2 |
| powder, for solution | 2 |
| solution, concentrate | 2 |
| solution | 1 |
| Route | NDCs |
|---|---|
| oral | 41 |
| intravenous | 2 |
| intramuscular | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| wilshire pharmaceuticals, inc. | 37 |
| wilshire pharmaceuticals | 9 |
| wilshire pharmaceuticals inc. | 2 |
Catalogue
Marketed products
48| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Amphetamine Sulfate | Amphetamine Sulfate | tablet, oral | 52536-057ANDA |
| Amphetamine Sulfate | Amphetamine Sulfate | tablet, oral | 52536-059ANDA |
| Azilsartan Medoxomil | Azilsartan kamedoxomil | tablet, oral | 52536-004NDA |
| Azilsartan Medoxomil | Azilsartan kamedoxomil | tablet, oral | 52536-008NDA |
| Baclofen | baclofen | suspension, oral | 52536-600NDA AUTHORIZED GENERIC |
| Carisoprodol | Carisoprodol | tablet, oral | 52536-682ANDA |
| Carisoprodol | Carisoprodol | tablet, oral | 52536-688ANDA |
| DEXMEDETOMIDINE HYDROCHLORIDE | dexmedetomidine hydrochloride | injection, intravenous | 52536-125ANDA |
| DEXMEDETOMIDINE HYDROCHLORIDE | dexmedetomidine hydrochloride | injection, intravenous | 52536-126ANDA |
| Dextroamphetamine Sulfate | Dextroamphetamine Sulfate | tablet, oral | 52536-500ANDA |
| Dextroamphetamine Sulfate | Dextroamphetamine Sulfate | tablet, oral | 52536-510ANDA |
| Dextroamphetamine Sulfate | Dextroamphetamine Sulfate | tablet, oral | 52536-515ANDA |
| Dextroamphetamine Sulfate | Dextroamphetamine Sulfate | tablet, oral | 52536-520ANDA |
| Dextroamphetamine Sulfate | Dextroamphetamine Sulfate | tablet, oral | 52536-530ANDA |
| ERYTHROMYCIN ETHYLSUCCINATE | Erythromycin Ethylsuccinate | suspension, oral | 52536-130NDA |
| ERYTHROMYCIN ETHYLSUCCINATE | Erythromycin Ethylsuccinate | suspension, oral | 52536-132NDA |
| Enalapril maleate | Enalapril maleate | solution, oral | 52536-401NDA |
| Erythromycin | Erythromycin | tablet, film coated, oral | 52536-103ANDA |
| Erythromycin | Erythromycin | tablet, film coated, oral | 52536-105ANDA |
| Erythromycin | Erythromycin | tablet, delayed release, oral | 52536-180ANDA |
| Erythromycin | Erythromycin | tablet, delayed release, oral | 52536-183ANDA |
| Erythromycin | Erythromycin | tablet, delayed release, oral | 52536-186ANDA |
| Erythromycin Ethylsuccinate | Erythromycin Ethylsuccinate | granule, for suspension, oral | 52536-134NDA |
| Erythromycin Ethylsuccinate | Erythromycin Ethylsuccinate | granule, for suspension, oral | 52536-136NDA |
| Lomustine | lomustine | capsule, gelatin coated, oral | 52536-340NDA |
| Lomustine | lomustine | capsule, gelatin coated, oral | 52536-341NDA |
| Lomustine | lomustine | capsule, gelatin coated, oral | 52536-342NDA |
| PEG 3350 and Electrolytes | Polyethylene Glycol 3350, Sodium Sulfate Anhydrous, Sodium Bicarbonate, Sodium Chloride, Potassium Chloride | powder, for solution, oral | 52536-236NDA AUTHORIZED GENERIC |
| PEG 3350, sodium chloride, sodium bicarbonate and potassium chloride | polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloride | powder, for solution, oral | 52536-302NDA AUTHORIZED GENERIC |
| Perphenazine | Perphenazine | tablet, film coated, oral | 52536-162ANDA |
| Perphenazine | Perphenazine | tablet, film coated, oral | 52536-164ANDA |
| Perphenazine | Perphenazine | tablet, film coated, oral | 52536-168ANDA |
| Perphenazine | Perphenazine | tablet, film coated, oral | 52536-170ANDA |
| SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE | sodium sulfate, potassium sulfate, magnesium sulfate | solution, concentrate, oral | 52536-175NDA |
| SODIUM SULFATE, POTASSIUM SULFATE AND MAGNESIUM SULFATE | sodium sulfate, potassium sulfate, magnesium sulfate | solution, concentrate, oral | 52536-177NDA |
| Testosterone Cypionate | testosterone cypionate | injection, intramuscular | 52536-625ANDA |
| Vancomycin Hydrochloride for Oral Solution | vancomycin hydrochloride | kit | 52536-104NDA AUTHORIZED GENERIC |
| Vancomycin Hydrochloride for Oral Solution | vancomycin hydrochloride | kit | 52536-106NDA AUTHORIZED GENERIC |
| Vancomycin Hydrochloride for Oral Solution | vancomycin hydrochloride | kit | 52536-107NDA AUTHORIZED GENERIC |
| Vancomycin Hydrochloride for Oral Solution | vancomycin hydrochloride | kit | 52536-108NDA AUTHORIZED GENERIC |
| Verapamil Hydrochloride | Verapamil Hydrochloride | capsule, extended release, oral | 52536-485NDA AUTHORIZED GENERIC |
| Verapamil Hydrochloride | Verapamil Hydrochloride | capsule, extended release, oral | 52536-486NDA AUTHORIZED GENERIC |
| Verapamil Hydrochloride | Verapamil Hydrochloride | capsule, extended release, oral | 52536-487NDA AUTHORIZED GENERIC |
| Verapamil Hydrochloride | verapamil hydrochloride | capsule, delayed release, oral | 52536-880NDA AUTHORIZED GENERIC |
| Verapamil Hydrochloride | verapamil hydrochloride | capsule, delayed release, oral | 52536-882NDA AUTHORIZED GENERIC |
| Verapamil Hydrochloride | verapamil hydrochloride | capsule, delayed release, oral | 52536-884NDA AUTHORIZED GENERIC |
| Verapamil Hydrochloride | verapamil hydrochloride | capsule, delayed release, oral | 52536-886NDA AUTHORIZED GENERIC |
| isosorbide dinitrate and hydralazine hydrochloride | hydralazine hydrochloride and isosorbide dinitrate | tablet, film coated, oral | 52536-006NDA AUTHORIZED GENERIC |
Compare
Other companies listing dextroamphetamine sulfate
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- Amneal Pharmaceuticals of New York, LLC14 sites · 227 NDC
- Siegfried USA, LLC12 sites · 54 NDC
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- KVK-TECH, INC.2 sites · 71 NDC
- Veranova, L.P.2 sites · 52 NDC
- Bryant Ranch Prepack1 site · 4,357 NDC
- Cranbury Pharmaceuticals Inc1 site · 44 NDC
- Chattem Chemicals, Inc.1 site · 35 NDC
- WINDER LABORATORIES, LLC1 site · 31 NDC
Enquiry
Common questions
- Is Wilshire Pharmaceuticals, Inc. FDA approved?
- Wilshire Pharmaceuticals, Inc. holds no registered establishment of its own; 48 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Wilshire Pharmaceuticals, Inc. make?
- 48 products are listed under Wilshire Pharmaceuticals, Inc. in the openFDA NDC Directory, most often as tablet; tablet, film coated; capsule, delayed 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.