NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4229Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4229Add 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 NDC11-digit (billing)PackageCopy
70518-4229-07051842290014 TABLET in 1 BOTTLE, PLASTIC (70518-4229-0)Marketed from Nov 11, 2024
70518-4229-17051842290120 TABLET in 1 BLISTER PACK (70518-4229-1)Marketed from Dec 11, 2024
70518-4229-27051842290220 TABLET in 1 BOTTLE, PLASTIC (70518-4229-2)Marketed from Jan 14, 2025
70518-4229-37051842290330 TABLET in 1 BLISTER PACK (70518-4229-3)Marketed from Jan 29, 2025
70518-4229-47051842290414 TABLET in 1 BLISTER PACK (70518-4229-4)Marketed from May 19, 2025
70518-4229-57051842290514 TABLET in 1 BOTTLE, PLASTIC (70518-4229-5)Marketed from Jul 9, 2025
70518-4229-67051842290630 TABLET in 1 BLISTER PACK (70518-4229-6)Marketed from Jul 31, 2025
70518-4229-77051842290730 TABLET in 1 BOTTLE, PLASTIC (70518-4229-7)Marketed from Jan 26, 2026
70518-4229-87051842290810 TABLET in 1 BOTTLE, PLASTIC (70518-4229-8)Marketed from Jul 28, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
ciprofolxacin
Active ingredients
Ciprofloxacin hydrochloride — 500 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208921
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 1A2 Inhibitors (Mechanism)Fluoroquinolones (Chemical structure)
Identifiers
Product ID 70518-4229_57bf0f26-da7e-a7aa-e063-6394a90aac36SPL ID 57bf0f26-da7e-a7aa-e063-6394a90aac36SPL set ID c527d138-e32c-418f-9573-a3d8a796279fRxCUI 309309UNII 4BA73M5E37

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

N470518422900 followed by a unit qualifier and the quantity

Package 70518-4229-00. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Click here to enter Indications 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 ) Acute E…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 208921

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

FDA NDC Directory listings under ANDA 208921
ProductStrengthForm · routeLabelerProduct NDC
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralCoupler LLC67046-1460
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-519
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3610
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralSt. Mary's Medical Park Pharmacy60760-676
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralNorthwind Health Company, LLC51655-490
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralAsclemed USA, Inc.76420-928
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralProficient Rx LP82804-130
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralAsclemed USA, Inc.76420-929
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-690
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-689
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralRedpharm Drug67296-2135
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-2097
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3901
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, CoatedOralMethod Pharmaceuticals, LLC58657-675
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0492
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralMethod Pharmaceuticals, LLC58657-676
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralRedpharm Drug67296-2169
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralCoupler LLC67046-1537
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, CoatedOralPreferred Pharmaceuticals Inc.68788-8200
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralBryant Ranch Prepack71335-2450

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