ciprofloxacin NDC 82868-102

NDC codes

FDA NDC Directory

Product NDC (as listed)82868-102Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82868-0102Add 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
82868-102-14	82868010214	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-102-14)Marketed from Feb 12, 2026
82868-102-20	82868010220	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-102-20)Marketed from Jul 21, 2026

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
Active ingredients: Ciprofloxacin hydrochloride — 250 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Northwind Health Company, LLC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076639
Marketing start: Feb 12, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 1A2 Inhibitors (Mechanism)Fluoroquinolones (Chemical structure)
Identifiers: Product ID 82868-102_575b7c88-3d25-1994-e063-6294a90a4997SPL ID 575b7c88-3d25-1994-e063-6294a90a4997SPL set ID 4deea61e-f3ca-b35d-e063-6294a90a9d41RxCUI 197511UNII 4BA73M5E37
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

N482868010214 followed by a unit qualifier and the quantity

Package 82868-0102-14. 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 Jul 21, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Ciprofloxacin is a fluoroquinolone antibacterial indicated in adults (18 years of age and older) 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 ) o Acute Exacerbation of Chronic Bronchi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 076639

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

FDA NDC Directory listings under ANDA 076639
Product	Strength	Form · route	Labeler	Product NDC
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-716
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	TabletOral	Proficient Rx LP	63187-990
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-919
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	QPharma, Inc.	42708-192
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-869
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Bryant Ranch Prepack	71335-0408
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	TabletOral	Coupler LLC	67046-1528
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	16571-413
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	PharmPak, Inc.	54348-662
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	16571-411
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	16571-412
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	PharmPak, Inc.	54348-663
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-0193
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-410
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Umasuto, LLC	85293-003
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Umasuto, LLC	85293-002
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	TabletOral	Umasuto, LLC	85293-004
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Bryant Ranch Prepack	71335-0070
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Proficient Rx LP	63187-017
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4122

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