Uzedy

risperidone · Injection, Suspension, Extended Release · Subcutaneous

Prescription (Rx) Atypical Antipsychotic

No FDA structured label text is available for Uzedy. The NDC listings below come from the FDA National Drug Code directory.

Active ingredients

Uzedy NDC products (7)

NDCStrength & formLabelerType
51759-305Risperidone 50 mg/.14mL
Injection, Suspension, Extended Release
Teva Pharmaceuticals USA, Inc.NDA
51759-410Risperidone 75 mg/.21mL
Injection, Suspension, Extended Release
Teva Pharmaceuticals USA, Inc.NDA
51759-520Risperidone 100 mg/.28mL
Injection, Suspension, Extended Release
Teva Pharmaceuticals USA, Inc.NDA
51759-630Risperidone 125 mg/.35mL
Injection, Suspension, Extended Release
Teva Pharmaceuticals USA, Inc.NDA
51759-740Risperidone 150 mg/.42mL
Injection, Suspension, Extended Release
Teva Pharmaceuticals USA, Inc.NDA
51759-850Risperidone 200 mg/.56mL
Injection, Suspension, Extended Release
Teva Pharmaceuticals USA, Inc.NDA
51759-960Risperidone 250 mg/.7mL
Injection, Suspension, Extended Release
Teva Pharmaceuticals USA, Inc.NDA

Frequently asked questions

Who makes Uzedy?

Uzedy is listed by 1 labeler in the FDA NDC directory, including Teva Pharmaceuticals USA, Inc..