NDC 71610-419 – Olanzapine

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

Human Prescription Drug

Product NDC71610-419

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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 (1)

Package NDCDescriptionSince
71610-419-3030 TABLET, FILM COATED in 1 BOTTLE (71610-419-30)Apr 23, 2020

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