NDC 55111-168 – Olanzapine

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

Human Prescription Drug

Product NDC55111-168

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
Dr. Reddy's Laboratories Ltd.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076133
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 (5)

Package NDCDescriptionSince
55111-168-01100 TABLET, FILM COATED in 1 BOTTLE (55111-168-01)Apr 23, 2012
55111-168-05500 TABLET, FILM COATED in 1 BOTTLE (55111-168-05)Apr 23, 2012
55111-168-3030 TABLET, FILM COATED in 1 BOTTLE (55111-168-30)Apr 23, 2012
55111-168-6060 TABLET, FILM COATED in 1 BOTTLE (55111-168-60)Apr 23, 2012
55111-168-7810 BLISTER PACK in 1 CARTON (55111-168-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (55111-168-79)Apr 23, 2012

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