NDC 60687-584 – Mirtazapine

Mirtazapine 7.5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC60687-584

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076921
Marketed since
August 29, 2022
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (1)

Package NDCDescriptionSince
60687-584-2130 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-584-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-584-11)Aug 29, 2022

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