NDC 70518-2337 – Olanzapine

Olanzapine 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-2337

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202862
Marketed since
October 2, 2019
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Olanzapine →

Package NDC codes (1)

Package NDCDescriptionSince
70518-2337-130 TABLET, FILM COATED in 1 BLISTER PACK (70518-2337-1)Aug 6, 2025

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