NDC 71205-749 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC71205-749

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Proficient Rx LP
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
August 12, 2020
Listing expires
December 31, 2026
Pharmacologic class
Quinolone Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (9)

Package NDCDescriptionSince
71205-749-055 TABLET, COATED in 1 BOTTLE (71205-749-05)Jan 26, 2023
71205-749-066 TABLET, COATED in 1 BOTTLE (71205-749-06)Jan 26, 2023
71205-749-1010 TABLET, COATED in 1 BOTTLE (71205-749-10)Jan 26, 2023
71205-749-1414 TABLET, COATED in 1 BOTTLE (71205-749-14)Jan 26, 2023
71205-749-2020 TABLET, COATED in 1 BOTTLE (71205-749-20)Jan 26, 2023
71205-749-2828 TABLET, COATED in 1 BOTTLE (71205-749-28)Jan 26, 2023
71205-749-3030 TABLET, COATED in 1 BOTTLE (71205-749-30)Jan 26, 2023
71205-749-6060 TABLET, COATED in 1 BOTTLE (71205-749-60)Jan 26, 2023
71205-749-9090 TABLET, COATED in 1 BOTTLE (71205-749-90)Jan 26, 2023

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