Ciprofloxacin 72189-0623-20

Package NDC

72189-0623-20

Manufacturer: Direct_rx
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 14, 2025
Listing Expires: December 31, 2027
Application: ANDA208921

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Active Ingredients

Ingredient	Strength
Ciprofloxacin Hydrochloride	500 mg/1

Drug Class

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

Selected Package

72189-0623-20Selected

20 TABLET in 1 BOTTLE (72189-623-20)

Other packages for this product(2)

72189-0623-10

10 TABLET in 1 BOTTLE (72189-623-10)

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72189-0623-14

14 TABLET in 1 BOTTLE (72189-623-14)

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