NDC 71335-0408 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0408

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076639
Marketed since
September 10, 2004
Listing expires
December 31, 2026
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0408-07 TABLET in 1 BOTTLE (71335-0408-0)May 4, 2022
71335-0408-120 TABLET in 1 BOTTLE (71335-0408-1)May 4, 2022
71335-0408-210 TABLET in 1 BOTTLE (71335-0408-2)May 4, 2022
71335-0408-314 TABLET in 1 BOTTLE (71335-0408-3)May 4, 2022
71335-0408-46 TABLET in 1 BOTTLE (71335-0408-4)May 4, 2022
71335-0408-530 TABLET in 1 BOTTLE (71335-0408-5)May 4, 2022
71335-0408-660 TABLET in 1 BOTTLE (71335-0408-6)May 4, 2022
71335-0408-712 TABLET in 1 BOTTLE (71335-0408-7)May 4, 2022
71335-0408-840 TABLET in 1 BOTTLE (71335-0408-8)May 4, 2022
71335-0408-990 TABLET in 1 BOTTLE (71335-0408-9)May 4, 2022

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