NDC 71335-1055 – Mirtazapine

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

Human Prescription Drug

Product NDC71335-1055

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
October 22, 2004
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1055-130 TABLET, FILM COATED in 1 BOTTLE (71335-1055-1)Jan 10, 2019
71335-1055-260 TABLET, FILM COATED in 1 BOTTLE (71335-1055-2)Dec 1, 2022
71335-1055-390 TABLET, FILM COATED in 1 BOTTLE (71335-1055-3)Apr 2, 2024
71335-1055-4120 TABLET, FILM COATED in 1 BOTTLE (71335-1055-4)Apr 2, 2024
71335-1055-515 TABLET, FILM COATED in 1 BOTTLE (71335-1055-5)Apr 2, 2024
71335-1055-6180 TABLET, FILM COATED in 1 BOTTLE (71335-1055-6)Apr 2, 2024
71335-1055-745 TABLET, FILM COATED in 1 BOTTLE (71335-1055-7)Apr 2, 2024
71335-1055-821 TABLET, FILM COATED in 1 BOTTLE (71335-1055-8)Apr 2, 2024

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