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ATOMOXETINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARMA GLOBAL · Approved 2012-05-11
Drug application
- FDA Application #
ANDA079020- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- ATOMOXETINE HYDROCHLORIDE
- Generic name
- Atomoxetine Hydrochloride
- Active ingredients
- ATOMOXETINE HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Marketing status
- None (Tentative Approval)
- Sponsor
- SUN PHARMA GLOBAL
- First approval
- 2012-05-11
Source
- Authoritative
- Drugs@FDA application overview
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