FDA
Prochlorperazine Edisylate
The FDA lists this product in 26 strengths and forms.
Composition
- Active ingredients
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/ML · InjectableANDA089605-001 · Discontinued
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/ML · InjectableANDA089638-001 · Discontinued
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/ML · InjectableANDA089675-001 · Discontinued
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/ML · InjectableANDA089903-001 · Prescription
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/ML · InjectableANDA040540-001 · Prescription
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/ML · InjectableANDA089251-001 · Discontinued
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/ML · InjectableANDA212257-001 · Prescription
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/ML · InjectableANDA214379-001 · Prescription
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/5ML · SyrupANDA088597-001 · Discontinued
- PROCHLORPERAZINE EDISYLATE EQ 5MG BASE/ML · Injectable
At a glance
- Brand name
- Prochlorperazine Edisylate
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Amneal
- Status
- Discontinued
- FDA approval
- 28 Nov 2022
- Application
- ANDA214192-001