NDC 65862-031 – Mirtazapine

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

Human Prescription Drug

Product NDC65862-031

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076921
Marketed since
October 22, 2004
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (6)

Package NDCDescriptionSince
65862-031-01100 TABLET, FILM COATED in 1 BOTTLE (65862-031-01)Oct 22, 2004
65862-031-05500 TABLET, FILM COATED in 1 BOTTLE (65862-031-05)Oct 22, 2004
65862-031-3030 TABLET, FILM COATED in 1 BOTTLE (65862-031-30)Oct 22, 2004
65862-031-3230 TABLET, FILM COATED in 1 BLISTER PACK (65862-031-32)Oct 22, 2004
65862-031-6060 TABLET, FILM COATED in 1 BOTTLE (65862-031-60)Oct 22, 2004
65862-031-9090 TABLET, FILM COATED in 1 BOTTLE (65862-031-90)Oct 22, 2004

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