NDC 60760-847 – Ciprofloxacin Hydrochloride

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

Human Prescription Drug

Product NDC60760-847

Product details

Brand name
Ciprofloxacin Hydrochloride
Generic name
Ciprofloxacin Hydrochloride
Labeler
St. Mary's Medical Park Pharmacy
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076593
Marketed since
September 17, 2026
Listing expires
December 31, 2027
Pharmacologic class
Fluoroquinolone Antibacterial

Active ingredients

Uses, dosage, side effects and warnings for Ciprofloxacin Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
60760-847-2020 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-847-20)Sep 17, 2026

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