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FDAAugust 21, 2015drug

Lamivudine Oral Solution, USP, 10 mg per 1 mL, 240 mL bottle (8 ounces), Rx only, Manufactured by: Silarx Pharmaceuticals, Inc. Carmel, NY 10512, NDC 54838-0566-70

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Labeling: Incorrect or Missing Lot and/or Exp. Date - Firm received a customer complaint that the expiration date printed on the unit carton (5/18) does not match the expiration date on the bottle label (5/17).

What to do

FDA enforcement status: Terminated

Brands named

silarx pharmaceuticalsilarx

UPCs

54838056670

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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