NDC 50742-339 – Tafluprost

Tafluprost .015 mg/mL · Solution/ Drops · Ophthalmic

Human Prescription Drug

Product NDC50742-339

Product details

Brand name
Tafluprost
Generic name
Tafluprost
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
Solution/ Drops
Route
Ophthalmic
Marketing category
ANDA · ANDA218002
Marketed since
December 18, 2024
Listing expires
December 31, 2026
Pharmacologic class
Prostaglandin Analog

Active ingredients

Uses, dosage, side effects and warnings for Tafluprost →

Package NDC codes (1)

Package NDCDescriptionSince
50742-339-306 POUCH in 1 CARTON (50742-339-30) / 5 VIAL, SINGLE-DOSE in 1 POUCH (50742-339-05) / .3 mL in 1 VIAL, SINGLE-DOSEDec 18, 2024

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