NDC codes

FDA NDC Directory
Product NDC (as listed)71335-2450Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-2450Add 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
71335-2450-0713352450007 TABLET in 1 BOTTLE (71335-2450-0)Marketed from Aug 15, 2024
71335-2450-17133524500114 TABLET in 1 BOTTLE (71335-2450-1)Marketed from Aug 15, 2024
71335-2450-27133524500230 TABLET in 1 BOTTLE (71335-2450-2)Marketed from Aug 15, 2024
71335-2450-37133524500320 TABLET in 1 BOTTLE (71335-2450-3)Marketed from Aug 15, 2024
71335-2450-47133524500460 TABLET in 1 BOTTLE (71335-2450-4)Marketed from Aug 15, 2024
71335-2450-5713352450056 TABLET in 1 BOTTLE (71335-2450-5)Marketed from Aug 15, 2024
71335-2450-67133524500610 TABLET in 1 BOTTLE (71335-2450-6)Marketed from Aug 15, 2024
71335-2450-77133524500728 TABLET in 1 BOTTLE (71335-2450-7)Marketed from Aug 15, 2024
71335-2450-871335245008100 TABLET in 1 BOTTLE (71335-2450-8)Marketed from Aug 15, 2024
71335-2450-97133524500940 TABLET in 1 BOTTLE (71335-2450-9)Marketed from Aug 15, 2024

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 71335-2450_a5fcba51-4ab6-4b4a-a73d-64dec62a2e52SPL ID a5fcba51-4ab6-4b4a-a73d-64dec62a2e52SPL set ID 2b8288a2-18bf-423c-b175-33174be729d4RxCUI 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

N471335245000 followed by a unit qualifier and the quantity

Package 71335-2450-00. 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 Infecti…

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/1TabletOralREMEDYREPACK INC.70518-4229
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

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