NDCFind

Ciprofloxacin Hydrochloride 83939-0002-03

Package NDC

83939-0002-03

Product NDC: 83939-0002

Manufacturer
Verityrx, Llc
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
May 23, 2024
Listing Expires
December 31, 2026
Application
ANDA076593
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Active Ingredients

IngredientStrength
Ciprofloxacin Hydrochloride500 mg/1

Drug Class

Cytochrome P450 1A2 Inhibitors [MoA]Fluoroquinolone Antibacterial [EPC]Fluoroquinolones [CS]

Selected Package

83939-0002-03Selected

100 POUCH in 1 BOX, UNIT-DOSE (83939-0002-3) / 1 TABLET, FILM COATED in 1 POUCH

Other packages for this product(2)

1 TABLET, FILM COATED in 1 POUCH (83939-0002-1)

50 POUCH in 1 BOX, UNIT-DOSE (83939-0002-2) / 1 TABLET, FILM COATED in 1 POUCH