NDC 72865-369 – Mirtazapine

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

Human Prescription Drug

Product NDC72865-369

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
XLCare Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA219721
Marketed since
October 2, 2025
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (3)

Package NDCDescriptionSince
72865-369-05500 TABLET, FILM COATED in 1 BOTTLE (72865-369-05)Oct 2, 2025
72865-369-101000 TABLET, FILM COATED in 1 BOTTLE (72865-369-10)Oct 2, 2025
72865-369-3030 TABLET, FILM COATED in 1 BOTTLE (72865-369-30)Oct 2, 2025

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