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
- 49884-250_b06f7f64-c457-4ca9-ad33-61efa6aec9b0
- Product NDC
- 49884-250
- Form
- CAPSULE
- Composition / generic term
- olanzapine and fuoxetine
- Labeler
- Par Health USA, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20121126
- Source listing expiry
- 20271231
Source-listed ingredients
- OLANZAPINE — 6 mg/1
- FLUOXETINE HYDROCHLORIDE — 25 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE in 1 BOTTLE, PLASTIC (49884-250-11) · 49884-250-11
Source and coverage
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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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