Ciprofloxacin (ciprofloxacin hydrochloride) NDC 61442-223

NDC codes

FDA NDC Directory

Product NDC (as listed)61442-223Labeler and product segments. Claims need a package NDC.

Product NDC at billing width61442-0223Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
61442-223-01	61442022301	100 TABLET, FILM COATED in 1 BOTTLE (61442-223-01)Marketed from Oct 10, 2009
61442-223-05	61442022305	500 TABLET, FILM COATED in 1 BOTTLE (61442-223-05)Marketed from Oct 10, 2009

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Ciprofloxacin
Generic name (nonproprietary): ciprofloxacin hydrochloride
Active ingredients: Ciprofloxacin hydrochloride — 500 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Carlsbad Technology, Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076126
Marketing start: Oct 10, 2009
Listing expires: Dec 31, 2026
Other FDA classes: Cytochrome P450 1A2 Inhibitors (Mechanism)Fluoroquinolones (Chemical structure)
Identifiers: Product ID 61442-223_2d6a2060-1f59-696d-e063-6394a90a2796SPL ID 2d6a2060-1f59-696d-e063-6394a90a2796SPL set ID 37527eca-115e-4582-88cd-bba851ac6069RxCUI 197511, 197512, 309309UNII 4BA73M5E37UPC 0361442222017, 0361442223014, 0361442224509
Pharmacologic class: Fluoroquinolone Antibacterial

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N461442022301 followed by a unit qualifier and the quantity

Package 61442-0223-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Feb 5, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Ciprofloxacin Tablets 250 mg, 500 mg, and 750 mg are a fluoroquinolone antibacterial indicated in adults (≥18 years of age) with the following infections caused by designated, susceptible bacteria and in pediatric patients where indicated: Skin and Skin Structure Infections ( 1.1 ) Bone and Joint Infections ( 1.2 ) Complicated Intra-Abdominal Infections ( 1.3 ) Infectious Diarrhea ( 1.4 ) Typhoid Fever (Enteric Fever) ( 1.5 ) Uncomplicated Cervical and Urethral Gonorrhea ( 1.6 ) Inhalational Anthrax post-exposure in adult and pediatric patients ( 1.7 ) Plague in adult and pediatric patients ( 1.8 ) Chronic Bacterial Prostatitis ( 1.9 ) Lower Respiratory Tract Infections ( 1.10 ) Acute Exacer…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076126

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 076126
Product	Strength	Form · route	Labeler	Product NDC
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-4600
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-1010
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-165
Ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-081
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-923
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-109
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 750 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-224
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	Carlsbad Technology, Inc.	61442-222
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-065
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 750 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-776
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	Golden State Medical Supply, Inc.	51407-775
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-997
Ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-547
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7581
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-1347
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-1740
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-1741