NDC 70518-1611 – Olanzapine

Olanzapine 7.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-1611

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076255
Marketed since
October 29, 2018
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Olanzapine →

Package NDC codes (2)

Package NDCDescriptionSince
70518-1611-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-1611-0)Oct 29, 2018
70518-1611-230 TABLET, FILM COATED in 1 BLISTER PACK (70518-1611-2)Feb 7, 2025

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