NDC 70518-4229 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-4229

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
November 11, 2024
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (9)

Package NDCDescriptionSince
70518-4229-014 TABLET in 1 BOTTLE, PLASTIC (70518-4229-0)Nov 11, 2024
70518-4229-120 TABLET in 1 BLISTER PACK (70518-4229-1)Dec 11, 2024
70518-4229-220 TABLET in 1 BOTTLE, PLASTIC (70518-4229-2)Jan 14, 2025
70518-4229-330 TABLET in 1 BLISTER PACK (70518-4229-3)Jan 29, 2025
70518-4229-414 TABLET in 1 BLISTER PACK (70518-4229-4)May 19, 2025
70518-4229-514 TABLET in 1 BOTTLE, PLASTIC (70518-4229-5)Jul 9, 2025
70518-4229-630 TABLET in 1 BLISTER PACK (70518-4229-6)Jul 31, 2025
70518-4229-730 TABLET in 1 BOTTLE, PLASTIC (70518-4229-7)Jan 26, 2026
70518-4229-810 TABLET in 1 BOTTLE, PLASTIC (70518-4229-8)Jul 28, 2026

Other ciprofloxacin products