Register entry
- Registered sites
- 0
- Active NDC listings
- 83
- Labeller names
- 6
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
8383 active NDC listings: 83 human prescription drug. By marketing category: ANDA 72, NDA AUTHORIZED GENERIC 9, NDA 1, UNAPPROVED DRUG OTHER 1.
| Dosage form | NDCs |
|---|---|
| tablet | 29 |
| tablet, film coated | 18 |
| solution | 9 |
| patch | 6 |
| capsule | 5 |
| cream | 2 |
| gel | 2 |
| ointment | 2 |
| powder, for solution | 2 |
| suspension | 2 |
| tablet, coated | 2 |
| tablet, delayed release | 2 |
| injection | 1 |
| tablet, extended release | 1 |
| Route | NDCs |
|---|---|
| oral | 68 |
| topical | 6 |
| transdermal | 6 |
| auricular (otic) | 1 |
| rectal | 1 |
| subcutaneous | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| trupharma, llc | 28 |
| trupharma llc | 27 |
| trupharma llc | 12 |
| trupharma, llc | 12 |
| trupharma, llc | 3 |
| trupharma llc. | 1 |
Catalogue
Marketed products
83| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| ACETAZOLAMIDE | ACETAZOLAMIDE | tablet, oral | 52817-200ANDA |
| ACETAZOLAMIDE | ACETAZOLAMIDE | tablet, oral | 52817-201ANDA |
| Acetic Acid | Acetic Acid | solution, auricular (otic) | 52817-816ANDA |
| Aminocaproic acid | Aminocaproic Acid | solution, oral | 52817-815ANDA |
| BACLOFEN | BACLOFEN | tablet, oral | 52817-318ANDA |
| BACLOFEN | BACLOFEN | tablet, oral | 52817-319ANDA |
| BACLOFEN | BACLOFEN | tablet, oral | 52817-320ANDA |
| BACLOFEN | BACLOFEN | tablet, oral | 52817-321ANDA |
| Baclofen | Baclofen | solution, oral | 52817-620NDA AUTHORIZED GENERIC |
| Betamethasone Dipropionate USP, 0.05% | Betamethasone Dipropionate USP, 0.05% | ointment, topical | 52817-824ANDA |
| Bisoprolol | Bisoprolol fumarate | tablet, film coated, oral | 52817-270ANDA |
| Bisoprolol | Bisoprolol fumarate | tablet, film coated, oral | 52817-271ANDA |
| Bisoprolol Fumarate | Bisoprolol Fumarate | tablet, film coated, oral | 52817-268ANDA |
| CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | tablet, film coated, oral | 52817-330ANDA |
| CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | tablet, film coated, oral | 52817-331ANDA |
| CYCLOBENZAPRINE HYDROCHLORIDE | cyclobenzaprine hydrochloride | tablet, film coated, oral | 52817-332ANDA |
| Carbidopa-levodopa | carbidopa and levodopa | tablet, oral | 52817-390ANDA |
| Carbidopa-levodopa | carbidopa and levodopa | tablet, oral | 52817-391ANDA |
| Carbidopa-levodopa | carbidopa and levodopa | tablet, oral | 52817-392ANDA |
| Clonazepam | Clonazepam | tablet, oral | 52817-305ANDA |
| Clonidine | Clonidine | tablet, extended release, oral | 52817-375NDA AUTHORIZED GENERIC |
| Clonidine Transdermal System USP, 0.1 mg/day | clonidine transdermal system | patch, transdermal | 52817-505NDA AUTHORIZED GENERIC |
| Clonidine Transdermal System USP, 0.1 mg/day | clonidine transdermal system | patch, transdermal | 52817-610NDA AUTHORIZED GENERIC |
| Clonidine Transdermal System USP, 0.2 mg/day | clonidine transdermal system | patch, transdermal | 52817-506NDA AUTHORIZED GENERIC |
| Clonidine Transdermal System USP, 0.2 mg/day | clonidine transdermal system | patch, transdermal | 52817-611NDA AUTHORIZED GENERIC |
| Clonidine Transdermal System USP, 0.3 mg/day | clonidine transdermal system | patch, transdermal | 52817-507NDA AUTHORIZED GENERIC |
| Clonidine Transdermal System USP, 0.3 mg/day | clonidine transdermal system | patch, transdermal | 52817-612NDA AUTHORIZED GENERIC |
| Clonidine hydrochloride | Clonidine hydrochloride | tablet, oral | 52817-180ANDA |
| Clonidine hydrochloride | Clonidine hydrochloride | tablet, oral | 52817-181ANDA |
| Clonidine hydrochloride | Clonidine hydrochloride | tablet, oral | 52817-182ANDA |
| Clonidine hydrochloride | Clonidine hydrochloride | tablet, oral | 52817-183ANDA |
| Clotrimazole Topical Solution USP, 1% | Clotrimazole Topical Solution USP, 1% | solution, topical | 52817-800ANDA |
| Cyproheptadine Hydrochloride | Cyproheptadine Hydrochloride | tablet, oral | 52817-210ANDA |
| Cyproheptadine Hydrochloride | Cyproheptadine Hydrochloride | tablet, oral | 52817-415ANDA |
| Dapsone | Dapsone Gel, 5% | gel, topical | 52817-831ANDA |
| Dapsone | Dapsone | gel, topical | 52817-832ANDA |
| Ethacrynic acid | Ethacrynic acid | tablet, oral | 52817-367ANDA |
| Glipizide | Glipizide | tablet, oral | 52817-385ANDA |
| Levocarnitine | Levocarnitine | solution, oral | 52817-830ANDA |
| METOPROLOL TARTRATE | METOPROLOL TARTRATE | tablet, oral | 52817-250ANDA |
| METOPROLOL TARTRATE | METOPROLOL TARTRATE | tablet, oral | 52817-251ANDA |
| METOPROLOL TARTRATE | METOPROLOL TARTRATE | tablet, oral | 52817-252ANDA |
| METOPROLOL TARTRATE | METOPROLOL TARTRATE | tablet, oral | 52817-253ANDA |
| METOPROLOL TARTRATE | METOPROLOL TARTRATE | tablet, oral | 52817-254ANDA |
| Metformin Hydrochloride Oral Solution | Metformin Hydrochloride | solution, oral | 52817-820ANDA |
| Metformin Hydrochloride Oral Solution | Metformin Hydrochloride | solution, oral | 52817-821ANDA |
| Metoprolol Tartrate | Metoprolol Tartrate | tablet, film coated, oral | 52817-358ANDA |
| Metoprolol Tartrate | Metoprolol Tartrate | tablet, film coated, oral | 52817-359ANDA |
| Metoprolol Tartrate | Metoprolol Tartrate | tablet, film coated, oral | 52817-360ANDA |
| Metoprolol Tartrate | Metoprolol Tartrate | tablet, film coated, oral | 52817-361ANDA |
| Metoprolol Tartrate | Metoprolol Tartrate | tablet, film coated, oral | 52817-362ANDA |
| Midodrine Hydrochloride | Midodrine Hydrochloride | tablet, oral | 52817-323ANDA |
| Midodrine Hydrochloride | Midodrine Hydrochloride | tablet, oral | 52817-324ANDA |
| Midodrine Hydrochloride | Midodrine Hydrochloride | tablet, oral | 52817-325ANDA |
| NITROGLYCERIN | Nitroglycerin | ointment, rectal | 52817-835ANDA |
| Naproxen | Naproxen | tablet, delayed release, oral | 52817-380ANDA |
| Naproxen | Naproxen | tablet, delayed release, oral | 52817-381ANDA |
| Oxazepam | Oxazepam | capsule, oral | 52817-290ANDA |
| Oxazepam | Oxazepam | capsule, oral | 52817-291ANDA |
| Oxazepam | Oxazepam | capsule, oral | 52817-292ANDA |
| Oxybutynin Chloride | oxybutynin chloride | tablet, oral | 52817-260ANDA |
| Oxybutynin Chloride | oxybutynin chloride | tablet, oral | 52817-261ANDA |
| Prednisolone | Prednisolone oral | solution, oral | 52817-860ANDA |
| Primidone | Primidone | tablet, oral | 52817-117ANDA |
| Ramelteon | Ramelteon | tablet, film coated, oral | 52817-235ANDA |
| SILDENAFIL | sildenafil | tablet, film coated, oral | 52817-340ANDA |
| SILDENAFIL | sildenafil | tablet, film coated, oral | 52817-341ANDA |
| SILDENAFIL | sildenafil | tablet, film coated, oral | 52817-342ANDA |
| Sapropterin Dihydrochloride | Sapropterin Dihydrochloride | powder, for solution, oral | 52817-850ANDA |
| Sapropterin Dihydrochloride | Sapropterin Dihydrochloride | powder, for solution, oral | 52817-851ANDA |
| Sildenafil Citrate | Sildenafil | tablet, film coated, oral | 52817-295ANDA |
| Sucralfate | Sucralfate Oral | suspension, oral | 52817-840ANDA |
| Tramadol Hydrochloride | Tramadol Hydrochloride | tablet, coated, oral | 52817-195ANDA |
| Tramadol Hydrochloride | Tramadol Hydrochloride | tablet, coated, oral | 52817-196ANDA |
| Tramadol Hydrochloride | tramadol hydrochloride | solution, oral | 52817-615NDA AUTHORIZED GENERIC |
| Trazodone Hydrochloride | Trazodone Hydrochloride | tablet, film coated, oral | 52817-395ANDA |
| Trazodone Hydrochloride | Trazodone Hydrochloride | tablet, film coated, oral | 52817-396ANDA |
| Triamcinolone Acetonide | triamcinolone acetonide | cream, topical | 52817-811ANDA |
| Triamterene | Triamterene Capsules | capsule, oral | 52817-364ANDA |
| Triamterene | Triamterene Capsules | capsule, oral | 52817-365ANDA |
| VERSACLOZ | Clozapine | suspension, oral | 52817-601NDA |
| apomorphine hydrocloride | APOMORPHINE HYDROCHLORIDE | injection, subcutaneous | 52817-720ANDA |
| hydrocortisone acetate pramoxine HCl | Hydrocortisone Acetate, Pramoxine HCl | cream, topical | 52817-817UNAPPROVED DRUG OTHER |
Compare
Other companies listing clonidine transdermal system
- Technomed Inc.0 sites · 6 NDC
Enquiry
Common questions
- Is TruPharma LLC. FDA approved?
- TruPharma LLC. holds no registered establishment of its own; 83 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does TruPharma LLC. make?
- 83 products are listed under TruPharma LLC. in the openFDA NDC Directory, most often as tablet; tablet, film coated; solution. 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.