NDC 43063-410 – Ciprofloxacin

Ciprofloxacin Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC43063-410

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
PD-Rx Pharmaceuticals, Inc.
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 (5)

Package NDCDescriptionSince
43063-410-066 TABLET in 1 BOTTLE, PLASTIC (43063-410-06)Jan 23, 2012
43063-410-1010 TABLET in 1 BOTTLE, PLASTIC (43063-410-10)Mar 1, 2017
43063-410-1212 TABLET in 1 BOTTLE, PLASTIC (43063-410-12)Dec 6, 2012
43063-410-1414 TABLET in 1 BOTTLE, PLASTIC (43063-410-14)Feb 8, 2013
43063-410-2020 TABLET in 1 BOTTLE, PLASTIC (43063-410-20)May 6, 2014

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