NDC codes

FDA NDC Directory
Product NDC (as listed)70518-2837Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-2837Add 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
70518-2837-47051828370414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2837-4)Marketed from Feb 5, 2023

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)
ciprofloxacin
Active ingredients
Ciprofloxacin hydrochloride — 250 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076558
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 1A2 Inhibitors (Mechanism)Fluoroquinolones (Chemical structure)
Identifiers
Product ID 70518-2837_57c4efae-23a1-9d06-e063-6394a90a4480SPL ID 57c4efae-23a1-9d06-e063-6394a90a4480SPL set ID c08b37c3-5f01-47ed-9508-02813bbd008bRxCUI 197511UNII 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

N470518283704 followed by a unit qualifier and the quantity

Package 70518-2837-04. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 076558

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

FDA NDC Directory listings under ANDA 076558
ProductStrengthForm · routeLabelerProduct NDC
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3063
CiprofloxacinCiprofloxacin hydrochloride 750 mg/1Tablet, Film coatedOralBryant Ranch Prepack63629-3868
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-086
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralHikma Pharmaceuticals USA Inc.0143-9927
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1867
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralHikma Pharmaceuticals USA Inc.0143-9928
CiprofloxacinCiprofloxacin hydrochloride 750 mg/1Tablet, Film coatedOralHikma Pharmaceuticals USA Inc.0143-9929
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-108
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-118
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-124
CiprofloxacinCiprofloxacin hydrochloride 750 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-125
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralGolden State Medical Supply, Inc.60429-042
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralDirectRx72189-300
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralDirectRx72189-304
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.72789-193
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-214

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