NDC 71335-2627 – Olanzapine

Olanzapine 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2627

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076255
Marketed since
December 10, 2013
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Olanzapine →

Package NDC codes (3)

Package NDCDescriptionSince
71335-2627-130 TABLET, FILM COATED in 1 BOTTLE (71335-2627-1)Jun 2, 2025
71335-2627-260 TABLET, FILM COATED in 1 BOTTLE (71335-2627-2)Jun 2, 2025
71335-2627-390 TABLET, FILM COATED in 1 BOTTLE (71335-2627-3)Jun 2, 2025

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