NDC 68084-528 – Olanzapine

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

Human Prescription Drug

Product NDC68084-528

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076133
Marketed since
May 7, 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
68084-528-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-528-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-528-11)May 7, 2012

Other Olanzapine products