NDC 71205-481 – Mirtazapine

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

Human Prescription Drug

Product NDC71205-481

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Proficient Rx LP
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 (3)

Package NDCDescriptionSince
71205-481-3030 TABLET, FILM COATED in 1 BOTTLE (71205-481-30)Oct 1, 2020
71205-481-6060 TABLET, FILM COATED in 1 BOTTLE (71205-481-60)Oct 1, 2020
71205-481-9090 TABLET, FILM COATED in 1 BOTTLE (71205-481-90)Oct 1, 2020

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