NDC 0378-3530 – Mirtazapine

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

Human Prescription Drug 1 recall

Product NDC0378-3530

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076122
Marketed since
June 20, 2003
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (3)

Package NDCDescriptionSince
0378-3530-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3530-01)Aug 2, 2016
0378-3530-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3530-05)Jun 20, 2003
0378-3530-9330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3530-93)Jun 20, 2003

Recalls mentioning this NDC

Other Mirtazapine products