NDC 67046-0319 – Mirtazapine

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

Human Prescription Drug

Product NDC67046-0319

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Coupler LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076921
Marketed since
August 21, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (1)

Package NDCDescriptionSince
67046-0319-330 TABLET, FILM COATED in 1 BLISTER PACK (67046-0319-3)Aug 21, 2026

Other Mirtazapine products