FDA recall D-0650-2017

Product

Quinapril Tablets USP 5 mg, 90 count bottles, Lupin Pharmaceuticals, Inc., Baltimore, MD --- NDC 68180-556-09

Reason for recall

Failed Impurities/Degradation Specifications; Impurity A

Distribution

Nationwide

Key facts

Status

Terminated

Initiation date

2015-12-07

Report date

2017-04-12

Termination date

2017-04-10

Voluntary/Mandated

Voluntary: Firm initiated

Location

Baltimore, MD, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0650-2017