← FDA Drug Approvals (Drugs@FDA)
ATOMOXETINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: ZYDUS PHARMS USA INC · Approved 2010-09-16
Drug application
- FDA Application #
ANDA079017- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- ATOMOXETINE HYDROCHLORIDE
- Generic name
- ATOMOXETINE
- Active ingredients
- ATOMOXETINE HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- ZYDUS PHARMS USA INC
- Manufacturer
- Zydus Pharmaceuticals USA Inc.
- First approval
- 2010-09-16
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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