NDC 71205-487 – Olanzapine

Olanzapine 15 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71205-487

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202862
Marketed since
August 22, 2014
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
71205-487-3030 TABLET, FILM COATED in 1 BOTTLE (71205-487-30)Oct 16, 2020
71205-487-6060 TABLET, FILM COATED in 1 BOTTLE (71205-487-60)Oct 16, 2020
71205-487-9090 TABLET, FILM COATED in 1 BOTTLE (71205-487-90)Oct 16, 2020

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