NDC 68071-2384 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet, Coated · Oral

Human Prescription Drug

Product NDC68071-2384

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Coated
Route
Oral
Marketing category
ANDA · ANDA208921
Marketed since
August 12, 2020
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for ciprofloxacin →

Package NDC codes (9)

Package NDCDescriptionSince
68071-2384-110 TABLET, COATED in 1 BOTTLE (68071-2384-1)Apr 9, 2021
68071-2384-220 TABLET, COATED in 1 BOTTLE (68071-2384-2)Apr 9, 2021
68071-2384-330 TABLET, COATED in 1 BOTTLE (68071-2384-3)Apr 9, 2021
68071-2384-414 TABLET, COATED in 1 BOTTLE (68071-2384-4)Apr 9, 2021
68071-2384-515 TABLET, COATED in 1 BOTTLE (68071-2384-5)Apr 9, 2021
68071-2384-660 TABLET, COATED in 1 BOTTLE (68071-2384-6)Apr 9, 2021
68071-2384-721 TABLET, COATED in 1 BOTTLE (68071-2384-7)Apr 9, 2021
68071-2384-828 TABLET, COATED in 1 BOTTLE (68071-2384-8)Apr 9, 2021
68071-2384-990 TABLET, COATED in 1 BOTTLE (68071-2384-9)Apr 9, 2021

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