NDC 71335-0286 – Mirtazapine

Mirtazapine 15 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0286

Product details

Brand name
Mirtazapine
Generic name
Mirtazapine
Labeler
Bryant Ranch Prepack
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 (8)

Package NDCDescriptionSince
71335-0286-130 TABLET in 1 BOTTLE (71335-0286-1)Sep 9, 2021
71335-0286-260 TABLET in 1 BOTTLE (71335-0286-2)Nov 8, 2021
71335-0286-390 TABLET in 1 BOTTLE (71335-0286-3)Dec 27, 2021
71335-0286-4120 TABLET in 1 BOTTLE (71335-0286-4)Dec 27, 2021
71335-0286-515 TABLET in 1 BOTTLE (71335-0286-5)Dec 27, 2021
71335-0286-6180 TABLET in 1 BOTTLE (71335-0286-6)Dec 27, 2021
71335-0286-745 TABLET in 1 BOTTLE (71335-0286-7)Dec 27, 2021
71335-0286-821 TABLET in 1 BOTTLE (71335-0286-8)Dec 27, 2021

Other Mirtazapine products