Moxifloxacin Hydrochloride 72789-0350-10

Package NDC

72789-0350-10

Manufacturer: Pd-Rx Pharmaceuticals, Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 4, 2014
Listing Expires: December 31, 2027
Application: ANDA202632

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Active Ingredients

Ingredient	Strength
Moxifloxacin Hydrochloride	400 mg/1

Drug Class

Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]

Selected Package

72789-0350-10Selected

10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-350-10)