NDC 50090-1058 – Mirtazapine

Mirtazapine 30 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC50090-1058

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077666
Marketed since
August 22, 2007
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (3)

Package NDCDescriptionSince
50090-1058-030 TABLET, FILM COATED in 1 BOTTLE (50090-1058-0)Nov 28, 2014
50090-1058-260 TABLET, FILM COATED in 1 BOTTLE (50090-1058-2)Nov 28, 2014
50090-1058-390 TABLET, FILM COATED in 1 BOTTLE (50090-1058-3)Nov 28, 2014

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