NDC 71610-523 – Mirtazapine

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

Human Prescription Drug

Product NDC71610-523

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076122
Marketed since
June 19, 2003
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (5)

Package NDCDescriptionSince
71610-523-1515 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-523-15)Apr 23, 2021
71610-523-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-523-30)Feb 3, 2021
71610-523-4545 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-523-45)Apr 23, 2021
71610-523-5360 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-523-53)Aug 4, 2021
71610-523-6090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-523-60)Feb 12, 2021

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