News
Glaucoma Drug Recalled
01/09/2020
The recall affects 7.5-mL bottles of bimatoprost (NDC 68180-429-03) from lot H801686 (Exp. 12/31/19). The bottles were distributed nationwide.
Lupin Pharmaceuticals initiated the voluntary recall December 13, 2019. On January 2, 2020, the FDA designated the recall Class III, suggesting use of the affected solution is unlikely to cause adverse health consequences.
Bimatoprost ophthalmic solution is available with a prescription to reduce pressure inside the eye from glaucoma.
—Jolynn Tumolo