NDC 50090-2800 – Mirtazapine

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

Human Prescription Drug

Product NDC50090-2800

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
A-S Medication Solutions
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 (2)

Package NDCDescriptionSince
50090-2800-030 TABLET, FILM COATED in 1 BOTTLE (50090-2800-0)Mar 2, 2017
50090-2800-190 TABLET, FILM COATED in 1 BOTTLE (50090-2800-1)Jan 19, 2017

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