NDC 71610-717 – Mirtazapine

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

Human Prescription Drug

Product NDC71610-717

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077666
Marketed since
August 22, 2007
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (2)

Package NDCDescriptionSince
71610-717-1515 TABLET, FILM COATED in 1 BOTTLE (71610-717-15)Jun 19, 2023
71610-717-6090 TABLET, FILM COATED in 1 BOTTLE (71610-717-60)Jun 29, 2023

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