Moxifloxacin Hydrochloride 70069-0081-01

Package NDC

70069-0081-01

Manufacturer: Somerset Therapeutics, Llc
Dosage Form: Solution/ Drops
Route: Ophthalmic
Product Type: Human Prescription Drug
Marketing Start: November 25, 2024
Listing Expires: December 31, 2026
Application: ANDA209698

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Active Ingredients

Ingredient	Strength
Moxifloxacin Hydrochloride	5 mg/mL

Drug Class

Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]

Selected Package

70069-0081-01Selected

1 BOTTLE in 1 CARTON (70069-081-01) / 3 mL in 1 BOTTLE