NDC 72162-2562 – Mirtazapine

Mirtazapine 7.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72162-2562

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076921
Marketed since
August 17, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (2)

Package NDCDescriptionSince
72162-2562-330 TABLET, FILM COATED in 1 BOTTLE (72162-2562-3)Nov 4, 2025
72162-2562-5500 TABLET, FILM COATED in 1 BOTTLE (72162-2562-5)Nov 4, 2025

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