NDC 68071-4989 – Mirtazapine

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

Human Prescription Drug

Product NDC68071-4989

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
NuCare Pharmaceuticals,Inc.
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 (1)

Package NDCDescriptionSince
68071-4989-330 TABLET, FILM COATED in 1 BOTTLE (68071-4989-3)Jul 25, 2019

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