NDC codes

FDA NDC Directory
Product NDC (as listed)0143-9929Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00143-9929Add 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
0143-9929-0100143992901100 TABLET, FILM COATED in 1 BOTTLE (0143-9929-01)Marketed from Jun 9, 2004
0143-9929-500014399295050 TABLET, FILM COATED in 1 BOTTLE (0143-9929-50)Marketed from Jun 9, 2004

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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 — 750 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 0143-9929_570d11c9-d12f-47fd-be83-37fa26d1262fSPL ID 570d11c9-d12f-47fd-be83-37fa26d1262fSPL set ID 3b3d22dc-df09-4910-8c9b-1204eeedbd68RxCUI 197511, 197512, 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

N400143992901 followed by a unit qualifier and the quantity

Package 00143-9929-01. 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

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 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 coatedOralREMEDYREPACK INC.70518-2837
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralAsclemed USA, Inc.76420-214

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