Register entry
- Registered sites
- 0
- Active NDC listings
- 2
- Live patents
- 0
- Countries
- 0
Catalogue
Drug listings by form and route
22 active NDC listings: 2 human prescription drug. By marketing category: ANDA 2.
| Dosage form | NDCs |
|---|---|
| injection, solution | 2 |
| Route | NDCs |
|---|---|
| intravenous | 2 |
| subcutaneous | 2 |
| Labeller name on the listing | NDCs |
|---|---|
| sagent pharmaceticals | 2 |
Catalogue
Marketed products
2| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Heparin Sodium | Heparin Sodium | injection, solution, intravenous, subcutaneous | 25021-400ANDA |
| Heparin Sodium | Heparin Sodium | injection, solution, intravenous, subcutaneous | 25021-402ANDA |
Compare
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Enquiry
Common questions
- Is Sagent Pharmaceticals FDA approved?
- Sagent Pharmaceticals holds no registered establishment of its own; 2 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
- What drugs does Sagent Pharmaceticals make?
- 2 products are listed under Sagent Pharmaceticals in the openFDA NDC Directory, most often as injection, 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.