NDC 0615-8246 – Olanzapine

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

Human Prescription Drug

Product NDC0615-8246

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
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 (1)

Package NDCDescriptionSince
0615-8246-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8246-39)Nov 2, 2018

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