Register entry
- Registered sites
- 0
- Active NDC listings
- 22
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
2222 active NDC listings: 22 human prescription drug. By marketing category: ANDA 20, NDA 1, NDA AUTHORIZED GENERIC 1.
| Dosage form | NDCs |
|---|---|
| tablet, film coated | 11 |
| capsule | 3 |
| for suspension | 2 |
| suspension | 2 |
| elixir | 1 |
| injection, solution | 1 |
| kit | 1 |
| solution | 1 |
| Route | NDCs |
|---|---|
| oral | 20 |
| intravenous | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| kanchan healthcare inc | 22 |
Catalogue
Marketed products
22| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| DEXAMETHASONE | DEXAMETHASONE | elixir, oral | 85742-004ANDA |
| Erythromycin ethylsuccinate | Erythromycin ethylsuccinate | for suspension, oral | 85742-029ANDA |
| Erythromycin ethylsuccinate | Erythromycin ethylsuccinate | for suspension, oral | 85742-030ANDA |
| Ethambutol Hydrochloride | Ethambutol Hydrochloride | tablet, film coated, oral | 85742-005NDA AUTHORIZED GENERIC |
| Ethambutol Hydrochloride | Ethambutol Hydrochloride | tablet, film coated, oral | 85742-006NDA |
| Lacosamide | Lacosamide | tablet, film coated, oral | 85742-008ANDA |
| Lacosamide | Lacosamide | tablet, film coated, oral | 85742-009ANDA |
| Lacosamide | Lacosamide | tablet, film coated, oral | 85742-010ANDA |
| Lacosamide | Lacosamide | tablet, film coated, oral | 85742-011ANDA |
| Lacosamide | Lacosamide | solution, oral | 85742-014ANDA |
| Metronidazole | Metronidazole | tablet, film coated, oral | 85742-024ANDA |
| Metronidazole | Metronidazole | tablet, film coated, oral | 85742-025ANDA |
| NYSTATIN | NYSTATIN | suspension, oral | 85742-013ANDA |
| Oxcarbazepine | Oxcarbazepine | suspension, oral | 85742-007ANDA |
| Ramelteon | Ramelteon | tablet, film coated, oral | 85742-023ANDA |
| Regadenoson | Regadenoson | injection, solution, intravenous | 85742-012ANDA |
| Tizanidine hydrochloride | Tizanidine hydrochloride | capsule, oral | 85742-031ANDA |
| Tizanidine hydrochloride | Tizanidine hydrochloride | capsule, oral | 85742-032ANDA |
| Tizanidine hydrochloride | Tizanidine hydrochloride | capsule, oral | 85742-033ANDA |
| VARENICLINE TARTRATE | VARENICLINE TARTRATE | tablet, film coated, oral | 85742-015ANDA |
| VARENICLINE TARTRATE | VARENICLINE TARTRATE | tablet, film coated, oral | 85742-016ANDA |
| VARENICLINE TARTRATE | VARENICLINE TARTRATE | kit | 85742-017ANDA |
Compare
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- Glenmark Pharmaceuticals Inc., USA9 sites · 383 NDC
- Indoco Remedies Limited7 sites · 58 NDC
- Aurobindo Pharma Limited6 sites · 1,453 NDC
- Fresenius Kabi USA, LLC6 sites · 561 NDC
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Enquiry
Common questions
- Is Kanchan Healthcare Inc FDA approved?
- Kanchan Healthcare Inc holds no registered establishment of its own; 22 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Kanchan Healthcare Inc make?
- 22 products are listed under Kanchan Healthcare Inc in the openFDA NDC Directory, most often as tablet, film coated; capsule; for suspension. 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.