Moxifloxacin Hydrochloride 68084-0722-65

Package NDC

68084-0722-65

Manufacturer: American Health Packaging
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 19, 2014
Listing Expires: December 31, 2026
Application: ANDA202632

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Active Ingredients

Ingredient	Strength
Moxifloxacin Hydrochloride	400 mg/1

Drug Class

Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]

Selected Package

68084-0722-65Selected

50 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-722-65) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-722-11)