NDC 0093-5503 – Olanzapine and Fluoxetine

Olanzapine 3 mg/1; Fluoxetine Hydrochloride 25 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC0093-5503

Product details

Brand name
Olanzapine and Fluoxetine
Generic name
Olanzapine and Fluoxetine
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA202074
Marketed since
April 10, 2013
Listing expires
December 31, 2027
Pharmacologic class
Atypical Antipsychotic; Serotonin Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Olanzapine and Fluoxetine →

Package NDC codes (1)

Package NDCDescriptionSince
0093-5503-5630 CAPSULE in 1 BOTTLE (0093-5503-56)Apr 10, 2013

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