NDC 70518-0180 – Mirtazapine

Mirtazapine 15 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-0180

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076921
Marketed since
January 26, 2017
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (1)

Package NDCDescriptionSince
70518-0180-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-0180-0)Jan 26, 2017

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