Safety Alerts & Recalls

What does this mean?

This recall for Ibudone was issued at a warehouse and pharmacy level only. The FDA and the manufacturer have determined that any recalled product that may have been dispensed to patients does not pose a significant health risk. If you take Ibudone (hydrocodone bitartrate and ibuprofen tablets), 5 mg/200 mg and are concerned, you should consult with your physician.

Vintage Pharmaceuticals LLC Recalls Single Lot of Ibudone, 5 mg/200 mg tablets

Vintage Pharmaceuticals LLC, has recalled a single lot of Ibudone (hydrocodone bitartrate and ibuprofen tablets), 5 mg/200 mg. Lot number T036K09A is being recalled because routine testing found that the amount of active ingredient was too low in tablets from this lot.

Ibudone contains the active ingredients hydrocodone and ibuprofen and is commonly used in the treatment of pain. Tablets containing hydrocodone and ibuprofen are made by several generic manufacturers. They are also available under the brand name Vicoprofen or Reprexain. This recall alert only applies to this single lot of Ibudone (hydrocodone bitartrate and ibuprofen tablets), 5 mg/200 mg. No other hydrocodone and ibuprofen products were involved in this recall.

To view the FDA notice about this recall, please visit: more information here

Source: FDA
Publication Date: 2010-07-30
Last Updated: 2010-08-01

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