NDC 16252-515 – Ciprofloxacin

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

Human Prescription Drug

Product NDC16252-515

Product details

Brand name
Ciprofloxacin
Generic name
Ciprofloxacin
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076794
Marketed since
November 1, 2006
Marketing end
August 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin →

Package NDC codes (1)

Package NDCDescriptionSince
16252-515-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (16252-515-01)Nov 1, 2006

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