United States · FDA National Drug Code directory

Mirtazapine

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
57237-013_ed2cd1df-697f-4e63-8097-7802be5eb6bb
Product NDC
57237-013
Form
TABLET, ORALLY DISINTEGRATING
Composition / generic term
Mirtazapine
Labeler
Rising Pharma Holdings, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20060228
Source listing expiry
20261231

Source-listed ingredients

  • MIRTAZAPINE — 45 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 5 BLISTER PACK in 1 CARTON (57237-013-06) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK · 57237-013-06

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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