NDC 13107-001 – Mirtazapine

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

Human Prescription Drug 3 recalls

Product NDC13107-001

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Aurolife Pharma LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076921
Marketed since
August 17, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (5)

Package NDCDescriptionSince
13107-001-01100 TABLET, FILM COATED in 1 BOTTLE (13107-001-01)Aug 17, 2009
13107-001-05500 TABLET, FILM COATED in 1 BOTTLE (13107-001-05)Aug 17, 2009
13107-001-3030 TABLET, FILM COATED in 1 BOTTLE (13107-001-30)Aug 17, 2009
13107-001-6060 TABLET, FILM COATED in 1 BOTTLE (13107-001-60)Aug 17, 2009
13107-001-9090 TABLET, FILM COATED in 1 BOTTLE (13107-001-90)Aug 17, 2009

Recalls mentioning this NDC

Other Mirtazapine products