NDC 71335-1332 – Mirtazapine

Mirtazapine 45 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1332

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, 2027

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (4)

Package NDCDescriptionSince
71335-1332-130 TABLET, FILM COATED in 1 BOTTLE (71335-1332-1)Sep 5, 2019
71335-1332-290 TABLET, FILM COATED in 1 BOTTLE (71335-1332-2)Apr 3, 2024
71335-1332-360 TABLET, FILM COATED in 1 BOTTLE (71335-1332-3)Apr 3, 2024
71335-1332-428 TABLET, FILM COATED in 1 BOTTLE (71335-1332-4)Apr 3, 2024

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