NDC 51407-836 – Lurasidone Hydrochloride

Lurasidone Hydrochloride 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51407-836

Product details

Brand name
Lurasidone Hydrochloride
Generic name
Lurasidone Hydrochloride
Labeler
Golden State Medical Supply, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA208058
Marketed since
September 4, 2019
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Lurasidone hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
51407-836-05500 TABLET, FILM COATED in 1 BOTTLE (51407-836-05)Feb 3, 2024

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