United States · FDA National Drug Code directory

Olanzapine and Fluoxetine

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
0093-5505_debcba63-033a-446f-a086-ccdf9d790662
Product NDC
0093-5505
Form
CAPSULE
Composition / generic term
Olanzapine and Fluoxetine
Labeler
Teva Pharmaceuticals USA, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20120619
Source listing expiry
20271231

Source-listed ingredients

  • OLANZAPINE — 6 mg/1
  • FLUOXETINE HYDROCHLORIDE — 50 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 CAPSULE in 1 BOTTLE (0093-5505-56) · 0093-5505-56

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Olanzapine and Fluoxetine — United States | Molindra Medicines