← FDA Drug Approvals (Drugs@FDA)
DULOXETINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: ALKEM LABS LTD · Approved 2015-08-26
Drug application
- FDA Application #
ANDA203197- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- DULOXETINE HYDROCHLORIDE
- Generic name
- DULOXETINE
- Active ingredients
- DULOXETINE HYDROCHLORIDE
- Dosage form
- CAPSULE, DELAYED REL PELLETS
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- ALKEM LABS LTD
- Manufacturer
- Ascend Laboratories, LLC
- First approval
- 2015-08-26
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown