← FDA Drug Approvals (Drugs@FDA)
DULOXETINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: AJANTA PHARMA LTD · Approved 2017-01-06
Drug application
- FDA Application #
ANDA208706- 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
- AJANTA PHARMA LTD
- Manufacturer
- Quallent Pharmaceuticals Health LLC
- First approval
- 2017-01-06
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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