NDC 33342-072 – Olanzapine

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

Human Prescription Drug 2 recalls

Product NDC33342-072

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202862
Marketed since
August 22, 2014
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Olanzapine →

Package NDC codes (5)

Package NDCDescriptionSince
33342-072-0730 TABLET, FILM COATED in 1 BOTTLE (33342-072-07)Aug 22, 2014
33342-072-11100 TABLET, FILM COATED in 1 BOTTLE (33342-072-11)Aug 22, 2014
33342-072-1210 BLISTER PACK in 1 CARTON (33342-072-12) / 10 TABLET, FILM COATED in 1 BLISTER PACKAug 22, 2014
33342-072-15500 TABLET, FILM COATED in 1 BOTTLE (33342-072-15)Aug 22, 2014
33342-072-441000 TABLET, FILM COATED in 1 BOTTLE (33342-072-44)Aug 22, 2014

Recalls mentioning this NDC

Other Olanzapine products