NDC 62756-232 – Loteprednol Etabonate

Loteprednol Etabonate 5 mg/mL · Suspension/ Drops · Ophthalmic

Human Prescription Drug 1 recall

Product NDC62756-232

Product details

Brand name
Loteprednol Etabonate
Generic name
Loteprednol Etabonate
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Suspension/ Drops
Route
Ophthalmic
Marketing category
ANDA · ANDA212450
Marketed since
May 1, 2021
Marketing end
December 31, 2026
Pharmacologic class
Corticosteroid

Active ingredients

Uses, dosage, side effects and warnings for Loteprednol Etabonate →

Package NDC codes (3)

Package NDCDescriptionSince
62756-232-551 BOTTLE in 1 CARTON (62756-232-55) / 10 mL in 1 BOTTLEMay 1, 2021
62756-232-561 BOTTLE in 1 CARTON (62756-232-56) / 15 mL in 1 BOTTLEMay 1, 2021
62756-232-901 BOTTLE in 1 CARTON (62756-232-90) / 5 mL in 1 BOTTLEMay 1, 2021

Recalls mentioning this NDC

Other Loteprednol Etabonate products