NDC 71610-115 – Mirtazapine

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

Human Prescription Drug

Product NDC71610-115

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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 (3)

Package NDCDescriptionSince
71610-115-1515 TABLET, FILM COATED in 1 BOTTLE (71610-115-15)Aug 9, 2018
71610-115-3030 TABLET, FILM COATED in 1 BOTTLE (71610-115-30)Aug 9, 2018
71610-115-6090 TABLET, FILM COATED in 1 BOTTLE (71610-115-60)Aug 9, 2018

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