NDC 50090-8019 – Mirtazapine

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

Human Prescription Drug

Product NDC50090-8019

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
A-S Medication Solutions
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 (1)

Package NDCDescriptionSince
50090-8019-030 TABLET, FILM COATED in 1 BOTTLE (50090-8019-0)Jul 20, 2026

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