NDC 57237-008 – Mirtazapine

Mirtazapine 15 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC57237-008

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Rising Pharma Holdings, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076921
Marketed since
October 22, 2004
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (2)

Package NDCDescriptionSince
57237-008-05500 TABLET, FILM COATED in 1 BOTTLE (57237-008-05)Oct 22, 2004
57237-008-3030 TABLET, FILM COATED in 1 BOTTLE (57237-008-30)Oct 22, 2004

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