NDC 72603-159 – Olanzapine

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

Human Prescription Drug

Product NDC72603-159

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
NorthStar RxLLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202862
Marketed since
July 5, 2023
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
72603-159-0130 TABLET, FILM COATED in 1 BOTTLE (72603-159-01)Jul 5, 2023
72603-159-02500 TABLET, FILM COATED in 1 BOTTLE (72603-159-02)Jul 5, 2023
72603-159-031000 TABLET, FILM COATED in 1 BOTTLE (72603-159-03)Jul 5, 2023

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