Aprepitant Capsules, USP 40 mg, 1 capsule Unit Blister Pack, Rx Only, Manufactured in India for:...

FDA Recall #D-0349-2019 — Class III — November 27, 2018

Recall #D-0349-2019 Date: November 27, 2018 Classification: Class III Status: Terminated

Product Description

Aprepitant Capsules, USP 40 mg, 1 capsule Unit Blister Pack, Rx Only, Manufactured in India for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430. UPC 368462583401. NDC 68462-583-40

Reason for Recall

Shortfill: Aprepitant capsules 40 mg is being recalled due to customer reports of missing capsule in the blister pack.

Recalling Firm

Glenmark Pharmaceuticals Inc., USA — Mahwah, NJ

Classification

Class III — Not likely to cause adverse health consequences.

Product Type

Drugs

Product Quantity

5,016 blister packs

Distribution

Nationwide

Code Information

Lot: 17180918, EXP June 2020

Status

Terminated

Voluntary / Mandated

Voluntary: Firm initiated