NDC 68084-121 – Mirtazapine

Mirtazapine 45 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68084-121

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
January 5, 2006
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Mirtazapine →

Package NDC codes (1)

Package NDCDescriptionSince
68084-121-01100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-121-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-121-11)Jan 5, 2006

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