Spravato
Esketamine Hydrochloride · Solution · Nasal
No FDA structured label text is available for Spravato. The NDC listings below come from the FDA National Drug Code directory.
Active ingredients
- Esketamine Hydrochloride in 1 product
Spravato NDC products (1)
| NDC | Strength & form | Labeler | Type |
|---|---|---|---|
| 50458-028 | Esketamine Hydrochloride 28 mg/.2mL Solution | Janssen Pharmaceuticals, Inc. | NDA · DEA CIII |
Frequently asked questions
Who makes Spravato?
Spravato is listed by 1 labeler in the FDA NDC directory, including Janssen Pharmaceuticals, Inc..