NDC 71335-2599 – Olanzapine

Olanzapine 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2599

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090798
Marketed since
April 23, 2012
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Olanzapine →

Package NDC codes (5)

Package NDCDescriptionSince
71335-2599-130 TABLET, FILM COATED in 1 BOTTLE (71335-2599-1)Jun 5, 2025
71335-2599-215 TABLET, FILM COATED in 1 BOTTLE (71335-2599-2)Jun 5, 2025
71335-2599-360 TABLET, FILM COATED in 1 BOTTLE (71335-2599-3)Jun 5, 2025
71335-2599-490 TABLET, FILM COATED in 1 BOTTLE (71335-2599-4)Jun 5, 2025
71335-2599-5120 TABLET, FILM COATED in 1 BOTTLE (71335-2599-5)Jun 5, 2025

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