FDA
Duloxetine Hydrochloride
The FDA lists this product in 60 strengths and forms.
Composition
- Active ingredients
- DULOXETINE HYDROCHLORIDE 60MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- DULOXETINE HYDROCHLORIDE EQ 60MG BASE · Capsule, delayed rel pelletsANDA090745-003 · Discontinued
- DULOXETINE HYDROCHLORIDE EQ 20MG BASE · Capsule, delayed rel pelletsANDA090745-001 · Discontinued
- DULOXETINE HYDROCHLORIDE EQ 30MG BASE · Capsule, delayed rel pelletsANDA090745-002 · Discontinued
- DULOXETINE HYDROCHLORIDE EQ 60MG BASE · Capsule, delayed rel pelletsANDA203088-003 · Prescription
- DULOXETINE HYDROCHLORIDE EQ 20MG BASE · Capsule, delayed rel pelletsANDA203088-001 · Prescription
- DULOXETINE HYDROCHLORIDE EQ 40MG BASE · Capsule, delayed rel pelletsANDA203088-004 · Prescription
- DULOXETINE HYDROCHLORIDE EQ 30MG BASE · Capsule, delayed rel pelletsANDA203088-002 · Prescription
- DULOXETINE HYDROCHLORIDE 30MG · Capsule, delayed releaseANDA090775-002 · Tentative approval
- DULOXETINE HYDROCHLORIDE 60MG · Capsule, delayed releaseANDA090775-003 · Tentative approval
- DULOXETINE HYDROCHLORIDE 20MG · Capsule, delayed release
At a glance
- Brand name
- Duloxetine Hydrochloride
- Route
- Oral
- Dosage form
- Capsule, delayed release
- Applicant
- Wockhardt
- Status
- Tentative approval
- FDA approval
- 6 Jul 2011
- Application
- ANDA090773-003