← FDA Drug Approvals (Drugs@FDA)
DULOXETINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: YAOPHARMA CO LTD · Approved 2019-08-16
Drug application
- FDA Application #
ANDA207219- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- DULOXETINE HYDROCHLORIDE
- Generic name
- DULOXETINE HYDROCHLORIDE
- Active ingredients
- DULOXETINE HYDROCHLORIDE
- Dosage form
- CAPSULE, DELAYED REL PELLETS
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- YAOPHARMA CO LTD
- Manufacturer
- Yaopharma Co., Ltd.
- First approval
- 2019-08-16
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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