NDC 67877-176 – Olanzapine

Olanzapine 15 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC67877-176

Product details

Brand name
Olanzapine
Generic name
Olanzapine
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202295
Marketed since
January 1, 2012
Listing expires
December 31, 2026
Pharmacologic class
Atypical Antipsychotic

Active ingredients

Uses, dosage, side effects and warnings for Olanzapine →

Package NDC codes (6)

Package NDCDescriptionSince
67877-176-01100 TABLET in 1 BOTTLE (67877-176-01)Jan 1, 2012
67877-176-101000 TABLET in 1 BOTTLE (67877-176-10)Jan 1, 2012
67877-176-3030 TABLET in 1 BOTTLE (67877-176-30)Jan 1, 2012
67877-176-327 TABLET in 1 BOTTLE (67877-176-32)Jan 1, 2012
67877-176-3510 BLISTER PACK in 1 CARTON (67877-176-35) / 10 TABLET in 1 BLISTER PACK (67877-176-33)Jan 1, 2012
67877-176-853 BLISTER PACK in 1 CARTON (67877-176-85) / 10 TABLET in 1 BLISTER PACK (67877-176-33)Jan 1, 2012

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