NDC 0615-8663 – Mirtazapine

Mirtazapine 7.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0615-8663

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA219919
Marketed since
May 14, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (2)

Package NDCDescriptionSince
0615-8663-0515 TABLET, FILM COATED in 1 BLISTER PACK (0615-8663-05)Sep 16, 2026
0615-8663-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8663-39)Sep 16, 2026

Other Mirtazapine products