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NELARABINE

ANDA · Abbreviated New Drug Application (Generic) · Sponsor: MEITHEAL · Approved 2023-01-10

Drug application

FDA Application #
ANDA216038
Application type
Abbreviated New Drug Application (Generic)
Brand name
NELARABINE
Generic name
NELARABINE
Active ingredients
NELARABINE
Dosage form
INJECTABLE
Route
INTRAVENOUS
Marketing status
Prescription
Sponsor
MEITHEAL
Manufacturer
Meitheal Pharmaceuticals Inc
First approval
2023-01-10

Source

Authoritative
Drugs@FDA application overview
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