Register entry
- Registered sites
- 0
- Active NDC listings
- 15
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
1515 active NDC listings: 15 human prescription drug. By marketing category: ANDA 14, NDA AUTHORIZED GENERIC 1.
| Dosage form | NDCs |
|---|---|
| tablet | 8 |
| tablet, film coated | 5 |
| capsule, extended release | 1 |
| tablet, delayed release | 1 |
| Route | NDCs |
|---|---|
| oral | 15 |
| Labeller name on the listing | NDCs |
|---|---|
| doc rx | 15 |
Catalogue
Marketed products
15| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Azithromycin | Azithromycin | tablet, film coated, oral | 69306-250ANDA |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride | capsule, extended release, oral | 69306-015NDA AUTHORIZED GENERIC |
| Cyclobenzaprine Hydrochloride | Cyclobenzaprine Hydrochloride | tablet, film coated, oral | 69306-872ANDA |
| Dexamethasone | Dexamethasone | tablet, oral | 69306-111ANDA |
| Dexamethasone | Dexamethasone | tablet, oral | 69306-112ANDA |
| Dexamethasone | Dexamethasone | tablet, oral | 69306-114ANDA |
| Diclofenac Potassium | diclofenac potassium | tablet, film coated, oral | 69306-750ANDA |
| Etodolac | Etodolac | tablet, film coated, oral | 69306-020ANDA |
| Ibuprofen and famotidine | Ibuprofen and famotidine | tablet, film coated, oral | 69306-266ANDA |
| METHYLPREDNISOLONE | METHYLPREDNISOLONE | tablet, oral | 69306-400ANDA |
| Metaxalone | Metaxalone | tablet, oral | 69306-100ANDA |
| Metaxalone | Metaxalone | tablet, oral | 69306-311ANDA |
| Methocarbamol | methocarbamol | tablet, oral | 69306-500ANDA |
| Methocarbamol | methocarbamol | tablet, oral | 69306-510ANDA |
| Naproxen and esomeprazole magnesium | Naproxen and esomeprazole magnesium | tablet, delayed release, oral | 69306-005ANDA |
Compare
Other companies listing dexamethasone
- Cardinal Health 418, Inc.34 sites · 833 NDC
- Zydus Lifesciences Limited12 sites · 717 NDC
- Apotex Inc.6 sites · 372 NDC
- Pharma Packaging Solutions, LLC dba Tjoapack, LLC5 sites · 667 NDC
- EUROAPI5 sites · 41 NDC
- Hikma Pharmaceuticals USA Inc.4 sites · 763 NDC
- International Medication Systems, Ltd.3 sites · 2,801 NDC
- MEDISCA Inc.2 sites · 305 NDC
- Symbiotec Pharmalab Limited2 sites · 53 NDC
- Bryant Ranch Prepack1 site · 4,357 NDC
Enquiry
Common questions
- Is Doc Rx FDA approved?
- Doc Rx 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 Doc Rx make?
- 15 products are listed under Doc Rx in the openFDA NDC Directory, most often as tablet; tablet, film 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.