Home / Recalls / Osmotica Pharmaceutical Corp / D-0110-2018

D-0110-2018 Class III Terminated

Recalled by Osmotica Pharmaceutical Corp — Marietta, GA

Recall Details

Product Type
Drugs
Report Date
December 27, 2017
Initiation Date
December 18, 2017
Termination Date
May 1, 2019
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
10064 bottles

Product Description

Methylphenidate Hydrochloride Extended-release Tablets, USP 27 mg, 100-count bottles, Rx Only, Trigen Laboratories, LLC. Bridgewater, NJ 08807, NDC 13811-707-10

Reason for Recall

Subpotent Drug

Distribution Pattern

Nationwide

Code Information

Lot #: 170027A, Exp. 02/2019

Other recalls by Osmotica Pharmaceutical Corp

  • D-0581-2018 Class III — Methylphenidate Hydrochloride Extended-release Tablets, USP, 36 mg, 100-count bo (February 28, 2018)
  • D-0111-2018 Class III — Methylphenidate Hydrochloride Extended-release Tablets, USP 54 mg, 100-count bot (December 18, 2017)
  • D-1067-2013 Class III — Venlafaxine (Venlafaxine Hydrochloride) extended release Tablets, 225 mg, packag (September 16, 2013)