NDC 0615-8269 – Mirtazapine

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

Human Prescription Drug

Product NDC0615-8269

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076921
Marketed since
August 17, 2009
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (2)

Package NDCDescriptionSince
0615-8269-0515 TABLET, FILM COATED in 1 BLISTER PACK (0615-8269-05)Feb 18, 2019
0615-8269-3930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8269-39)Feb 18, 2019

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