NDC 72603-558 – Mirtazapine

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

Human Prescription Drug

Product NDC72603-558

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
NorthStar Rx LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076921
Marketed since
April 1, 2025
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (2)

Package NDCDescriptionSince
72603-558-0130 TABLET, FILM COATED in 1 BOTTLE (72603-558-01)Apr 1, 2025
72603-558-02500 TABLET, FILM COATED in 1 BOTTLE (72603-558-02)Apr 1, 2025

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