NDC 70518-4133 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-4133

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
July 3, 2024
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (4)

Package NDCDescriptionSince
70518-4133-030 TABLET in 1 BLISTER PACK (70518-4133-0)Jul 3, 2024
70518-4133-110 TABLET in 1 BOTTLE, PLASTIC (70518-4133-1)Oct 6, 2024
70518-4133-26 TABLET in 1 BOTTLE, PLASTIC (70518-4133-2)Apr 13, 2026
70518-4133-350 POUCH in 1 BOX (70518-4133-3) / 1 TABLET in 1 POUCH (70518-4133-4)Apr 24, 2026

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