NDC 55154-6889 – Olanzapine

Olanzapine 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC55154-6889

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
Cardinal Health 107, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076255
Marketed since
April 23, 2012
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Olanzapine →

Package NDC codes (1)

Package NDCDescriptionSince
55154-6889-010 BLISTER PACK in 1 BAG (55154-6889-0) / 1 TABLET, FILM COATED in 1 BLISTER PACKApr 23, 2012

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