FDAFDA · Alimentos y medicamentos·N.º oficial D-1041-2018

Diazepam Rectal Gel, 2.5 mg, TWIN PACK that Contains two pre-filled, unit-dose, rectal delivery systems with lubricating jelly and instructions for use per carton, Rx only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807; Manufactured by: DPT Laboratories, Ltd., San Antonio, TX 78215; NDC 68682-650-20.

Name: Diazepam Rectal Gel, 2.5 mg, TWIN PACK that Contains two pre-filled, unit-dose, rectal delivery systems with lubricating jelly and instructions for use per carton, Rx only, Manufactured for: Oceanside Pharmaceuticals, a division of Valeant Pharmaceuticals North America LLC, Bridgewater, NJ 08807; Manufactured by: DPT Laboratories, Ltd., San Antonio, TX 78215; NDC 68682-650-20.
Brand: DIAZEPAM

Publicado el 15 de agosto de 2018 · Inicio del retiro: 10 de julio de 2018

Estado reportado al momento de publicación: Terminated — openFDA actualiza semanalmente y este campo no refleja el estado más reciente. Confirma siempre con la fuente oficial.

Qué peligro representa

Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.

Qué hacer

Voluntary: Firm initiated · Letter

Detalles del retiro

Marca: DIAZEPAM
Fabricante: Valeant Pharmaceuticals North America LLC
Distribuidor: Nationwide in the USA
Lote: Lot #: NBBN, Exp 02/22
Clasificación de riesgo: Class III
Área (FDA): drug
País: United States