NDC 68084-723 – Olanzapine

Olanzapine 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68084-723

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076255
Marketed since
May 9, 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
68084-723-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-723-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-723-11)May 9, 2014

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