NDC 71335-0964 – Mirtazapine

Mirtazapine 30 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0964

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 (7)

Package NDCDescriptionSince
71335-0964-130 TABLET, FILM COATED in 1 BOTTLE (71335-0964-1)Oct 8, 2018
71335-0964-256 TABLET, FILM COATED in 1 BOTTLE (71335-0964-2)Apr 9, 2024
71335-0964-315 TABLET, FILM COATED in 1 BOTTLE (71335-0964-3)Aug 10, 2020
71335-0964-490 TABLET, FILM COATED in 1 BOTTLE (71335-0964-4)Aug 8, 2019
71335-0964-560 TABLET, FILM COATED in 1 BOTTLE (71335-0964-5)Apr 9, 2024
71335-0964-628 TABLET, FILM COATED in 1 BOTTLE (71335-0964-6)Apr 9, 2024
71335-0964-745 TABLET, FILM COATED in 1 BOTTLE (71335-0964-7)Apr 9, 2024

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