NDC 76420-928 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76420-928

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofolxacin
Labeler
Asclemed USA, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
October 1, 2023
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (6)

Package NDCDescriptionSince
76420-928-01100 TABLET in 1 BOTTLE (76420-928-01)Mar 28, 2025
76420-928-1414 TABLET in 1 BOTTLE (76420-928-14)May 29, 2026
76420-928-2020 TABLET in 1 BOTTLE (76420-928-20)Mar 28, 2025
76420-928-3030 TABLET in 1 BOTTLE (76420-928-30)Mar 28, 2025
76420-928-6060 TABLET in 1 BOTTLE (76420-928-60)Mar 28, 2025
76420-928-9090 TABLET in 1 BOTTLE (76420-928-90)Mar 28, 2025

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