Register entry
- Registered sites
- 0
- Active NDC listings
- 15
- Labeller names
- 6
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
1515 active NDC listings: 15 human prescription drug. By marketing category: ANDA 11, NDA 3, NDA AUTHORIZED GENERIC 1.
| Dosage form | NDCs |
|---|---|
| cream | 4 |
| tablet | 4 |
| solution | 2 |
| tablet, delayed release | 2 |
| tablet, film coated | 2 |
| tablet, coated | 1 |
| Route | NDCs |
|---|---|
| oral | 10 |
| topical | 5 |
| Labeller name on the listing | NDCs |
|---|---|
| ina pharmaceutics inc | 8 |
| ina pharmaceutics inc. | 2 |
| ina pharmaceutics, inc | 2 |
| ina pharmaceutics inc, | 1 |
| ina pharmaceutics inc. | 1 |
| ina pharmaceutics, inc. | 1 |
Catalogue
Marketed products
15| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Amcinonide | Amcinonide | cream, topical | 74157-006ANDA |
| CORDRAN | Flurandrenolide | cream, topical | 74157-130NDA |
| CORDRAN | Flurandrenolide | cream, topical | 74157-180NDA |
| Clobetasol Propionate | clobetasol propionate | cream, topical | 74157-710NDA AUTHORIZED GENERIC |
| DICLOFENAC POTASSIUM | diclofenac potassium, film coated | tablet, oral | 74157-016ANDA |
| Desloratadine Oral Solution | Desloratadine | solution, oral | 74157-011ANDA |
| Diclofenac Potassium | diclofenac potassium | tablet, coated, oral | 74157-007ANDA |
| Dolobid | Diflunisal | tablet, film coated, oral | 74157-009ANDA |
| Dolobid | Diflunisal | tablet, film coated, oral | 74157-101ANDA |
| GABARONE | Gabapentin | tablet, oral | 74157-013ANDA |
| GABARONE | Gabapentin | tablet, oral | 74157-111ANDA |
| Halcinonide Topical Solution | Halcinonide Topical | solution, topical | 74157-012ANDA |
| Metaxalone | Metaxalone | tablet, oral | 74157-018NDA |
| Prednisone delayed release | Prednisone | tablet, delayed release, oral | 74157-010ANDA |
| Prednisone delayed release | Prednisone | tablet, delayed release, oral | 74157-019ANDA |
Compare
Other companies listing diflunisal
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- Teva Pharmaceutical Industries Ltd.6 sites · 668 NDC
- Cohance Lifesciences Limited6 sites · 74 NDC
- AARTI PHARMALABS LIMITED3 sites · 34 NDC
- Zydus Pharmaceuticals USA Inc.1 site · 626 NDC
- Chartwell RX, LLC.0 sites · 580 NDC
Enquiry
Common questions
- Is INA Pharmaceutics, Inc. FDA approved?
- INA Pharmaceutics, Inc. holds no registered establishment of its own; 15 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does INA Pharmaceutics, Inc. make?
- 15 products are listed under INA Pharmaceutics, Inc. in the openFDA NDC Directory, most often as cream; tablet; 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.