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
- 13107-001_4329eeed-8071-4b6c-887d-0cd00647b84c
- Product NDC
- 13107-001
- Form
- TABLET, FILM COATED
- Composition / generic term
- Mirtazapine
- Labeler
- Aurolife Pharma LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20090817
- Source listing expiry
- 20261231
Source-listed ingredients
- MIRTAZAPINE — 7.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (13107-001-01) · 13107-001-01
- 500 TABLET, FILM COATED in 1 BOTTLE (13107-001-05) · 13107-001-05
- 30 TABLET, FILM COATED in 1 BOTTLE (13107-001-30) · 13107-001-30
- 60 TABLET, FILM COATED in 1 BOTTLE (13107-001-60) · 13107-001-60
- 90 TABLET, FILM COATED in 1 BOTTLE (13107-001-90) · 13107-001-90
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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