FDA NDC

Lurasidone Hydrochloride

This name is from the loaded FDA file.

Source: FDA NDC Directory, live from openFDA. Publisher page

NDC
47335-684
Proprietary name
Lurasidone Hydrochloride
Nonproprietary name
Lurasidone Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
TABLET
Strength
40 mg/1

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