NDC 69315-308 – Ciprofloxacin

Ciprofloxacin Hydrochloride 3 mg/mL · Solution · Ophthalmic

Human Prescription Drug 3 recalls

Product NDC69315-308

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Leading Pharma, LLC
Dosage form
Solution
Route
Ophthalmic
Marketing category
ANDA · ANDA077568
Marketed since
November 1, 2018
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (3)

Package NDCDescriptionSince
69315-308-021 BOTTLE, PLASTIC in 1 CARTON (69315-308-02) / 2.5 mL in 1 BOTTLE, PLASTICNov 1, 2018
69315-308-051 BOTTLE, PLASTIC in 1 CARTON (69315-308-05) / 5 mL in 1 BOTTLE, PLASTICNov 1, 2018
69315-308-101 BOTTLE, PLASTIC in 1 CARTON (69315-308-10) / 10 mL in 1 BOTTLE, PLASTICNov 1, 2018

Recalls mentioning this NDC

Other Ciprofloxacin products