Tafluprost 50742-0339-30

Package NDC

50742-0339-30

Manufacturer: Ingenus Pharmaceuticals, Llc
Dosage Form: Solution/ Drops
Route: Ophthalmic
Product Type: Human Prescription Drug
Marketing Start: December 18, 2024
Listing Expires: December 31, 2026
Application: ANDA218002

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Active Ingredients

Ingredient	Strength
Tafluprost	.015 mg/mL

Drug Class

Prostaglandin Analog [EPC]Increased Prostaglandin Activity [PE]Prostaglandin Analog [EPC]

Selected Package

50742-0339-30Selected

6 POUCH in 1 CARTON (50742-339-30) / 5 VIAL, SINGLE-DOSE in 1 POUCH (50742-339-05) / .3 mL in 1 VIAL, SINGLE-DOSE