NDC 57664-499 – Mirtazapine

Mirtazapine 15 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC57664-499

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076541
Marketed since
April 22, 2004
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (2)

Package NDCDescriptionSince
57664-499-181000 TABLET in 1 BOTTLE (57664-499-18)Apr 22, 2017
57664-499-8330 TABLET in 1 BOTTLE (57664-499-83)Apr 22, 2004

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