July 18, 2000Vicoprofen Tablets Tablets
Recalled by Knoll Pharmaceutical Company
Olive, NJ (SafetyAlerts) - The Food
and Drug Administration (FDA) today reported that Knoll Pharmaceutical Company is
conducting a recall of certain Vicoprofen(r) Tablets because some bottles have partially
illegible lot numbers and/or expiration dates.
Vicoprofen(r) Tablets (hydrocodone bitartrate 7.5 mg and ibuprofen 200 mg), in 500-count
NDC #0044-723-03. Recall #D-428-0. Class III
Lot #0000060685 EXP 10/01.
Knoll Pharmaceutical Company, Whippahy, New Jersey.
Knoll Pharmaceutical Company, Mt. Olive, New Jersey, by letter on April 28, 2000.
Firm-initiated recall ongoing. This is the first public notice issued by the FDA.
3,475 bottles were distributed.
Questions concerning this recall may be directed
to the FDA at 1-888-INFO-FDA.
Notice of this product warning was sent via email
to SafeMail subscribers July 18,
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