NDC 63187-017 – Ciprofloxacin

Ciprofloxacin Hydrochloride 500 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63187-017

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076639
Marketed since
September 10, 2004
Listing expires
December 31, 2026
Pharmacologic class
Quinolone Antimicrobial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (8)

Package NDCDescriptionSince
63187-017-066 TABLET in 1 BOTTLE (63187-017-06)Aug 1, 2014
63187-017-1010 TABLET in 1 BOTTLE (63187-017-10)Aug 1, 2014
63187-017-1414 TABLET in 1 BOTTLE (63187-017-14)Aug 1, 2014
63187-017-2020 TABLET in 1 BOTTLE (63187-017-20)Aug 1, 2014
63187-017-2828 TABLET in 1 BOTTLE (63187-017-28)Aug 4, 2016
63187-017-3030 TABLET in 1 BOTTLE (63187-017-30)Aug 1, 2014
63187-017-6060 TABLET in 1 BOTTLE (63187-017-60)Jul 23, 2021
63187-017-9090 TABLET in 1 BOTTLE (63187-017-90)Jul 23, 2021

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