RecallRadar

FDA Drug recall D-0520-2016

Norpace CR (disopyramide phosphate) extended-release capsules USP,150 mg, packaged in a) 100-count bottles (NDC 0025-2742-31), and b) 500-c…

On 2015-12-16 the FDA classified a Class III recall of Norpace CR (disopyramide phosphate) extended-release capsules USP,150 mg, packaged in a) 100-count bottles (NDC 0025-2742-31), and b) 500-c… by Pfizer, citing failed Dissolution Specification.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-0520-2016
ClassificationClass III
Statusterminated
Initiated2015-12-02
Published2015-12-16
Last updated2026-09-13 11:51 UTC
CompanyPfizer
DistributionUS

Product

Norpace CR (disopyramide phosphate) extended-release capsules USP,150 mg, packaged in a) 100-count bottles (NDC 0025-2742-31), and b) 500-count bottles (NDC 0025-2742-51), Rx only, Distributed by G.D. Searle LLC, Division of Pfizer Inc, NY, NY 10017.

Reason

Failed Dissolution Specification

Identifiers

ndc0025-2752-31
ndc0025-2762-31
ndc0025-2732-31
ndc0025-2742-31
ndc0025-2742-51
code_infoLot #: C150065; C150064, Exp 6/16

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0520-2016%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.