NDC 51407-352 – Mirtazapine

Mirtazapine 45 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC51407-352

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Golden State Medical Supply, Inc.
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 (2)

Package NDCDescriptionSince
51407-352-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-352-05)Feb 21, 2020
51407-352-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-352-30)Feb 21, 2020

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