FDA recall D-138-2013

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals · Class I · drug

Product

Hydrocodone bitartrate and acetaminophen Tablets, USP, 10 mg/500 mg, packaged in a) 30-count bottles, NDC 0603-3888-16; b) 60-count bottles, NDC 0603-3888-20; c) 90-count bottles, NDC 0603-3888-02; d) 100-count bottles, NDC 0603-3888-21; e) 120-count bottles, NDC 0603-3888-22; f) 150-count bottles, NDC 0603-3888-26; g) 180-count bottles, NDC 0603-3888-04; h) 500-count bottles, NDC 0603-3888-28; and i) 1000-count bottles, NDC 0603-3888-32, Rx only, Mfg. for: Qualitest Pharmaceuticals, Huntsville, AL 35811.

Reason for recall

Superpotent (Multiple Ingredient) Drug: Complaint received of oversized tablets.

Distribution

Nationwide and Puerto Rico

Key facts

Status: Terminated
Initiation date: 2012-12-06
Report date: 2013-02-06
Termination date: 2021-07-20
Voluntary/Mandated: Voluntary: Firm initiated
Location: Huntsville, AL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-138-2013