← FDA Drug Approvals (Drugs@FDA)
NILOTINIB HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: APOTEX · Approved 2024-01-05
Drug application
- FDA Application #
ANDA203640- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- NILOTINIB HYDROCHLORIDE
- Generic name
- NILOTINIB
- Active ingredients
- NILOTINIB HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- APOTEX
- Manufacturer
- Apotex Corp.
- First approval
- 2024-01-05
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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