NDC codes

FDA NDC Directory
Product NDC (as listed)72189-616Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0616Add 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
72189-616-06721890616066 TABLET in 1 BOTTLE (72189-616-06)Marketed from Feb 25, 2025

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
Route
Oral
Labeler
Direct_RxNDC labeler code 72189
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 72189-616_2efbda2a-fc98-b7c5-e063-6294a90a362dSPL ID 2efbda2a-fc98-b7c5-e063-6294a90a362dSPL set ID 2efbda2a-fc97-b7c5-e063-6294a90a362dRxCUI 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

N472189061606 followed by a unit qualifier and the quantity

Package 72189-0616-06. 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 1.1 Skin and Skin Structure Infections Ciprofloxacin tablets are indicated in adult patients for treatment of skin and skin structure infections caused by Escherichia coli, Klebsiella pneumoniae, Enterobacter cloacae, Proteus mirabilis, Proteus vulgaris, Providencia stuartii, Morganella morganii, Citrobacter freundii, Pseudomonas aeruginosa, methicillin-susceptible Staphylococcus aureus, methicillin-susceptible Staphylococcus epidermidis, or Streptococcus pyogenes. 1.2 Bone and Joint Infections Ciprofloxacin tablets are indicated in adult patients for treatment of bone and joint infections caused by Enterobacter cloacae, Serratia marcescens, or Pseudomonas aer…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-616

What is NDC 72189-616?
72189-616 is the product NDC for Ciprofloxacin, Ciprofloxacin hydrochloride 250 mg/1 tablet, listed with the FDA by Direct_Rx. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ciprofloxacin.
What is the active ingredient?
Ciprofloxacin hydrochloride.
Who is the labeler?
Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ciprofloxacin?
169 other product NDCs are listed under this name. See all Ciprofloxacin NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Ciprofloxacin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-94760687-0947-01
ciprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC82868-10282868-0102-1482868-0102-20
ciprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-019355154-0193-00
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralDirect_Rx72189-62772189-0627-1072189-0627-14
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-887568788-8875-0068788-8875-0168788-8875-02+4 more
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1TabletOralDirect_Rx72189-62372189-0623-1072189-0623-1472189-0623-20
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-69060760-0690-10
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralNCS HealthCare of KY, LLC dba Vangard Labs0615-863000615-8630-1000615-8630-1400615-8630-20
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 500 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-97759651-0977-0159651-0977-0559651-0977-20+2 more
Ciprofloxacinciprofloxacin hydrochlorideCiprofloxacin hydrochloride 250 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-97659651-0976-0159651-0976-2059651-0976-30+1 more

All 170 Ciprofloxacin NDCs

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
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralRedpharm Drug67296-1848
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, CoatedOralDirect Rx72189-323
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralA-S Medication Solutions50090-7297
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralAdvanced Rx of Tennessee, LLC80425-0492
Ciprofloxacinciprofloxacin tabletsCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralYiling Pharmaceutical, Inc.69117-0009
Ciprofloxacinciprofloxacin tabletsCiprofloxacin hydrochloride 250 mg/1Tablet, CoatedOralYiling Pharmaceutical, Inc.69117-0008
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1TabletOralDirect_Rx72189-623
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralCoupler LLC67046-1460
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralBryant Ranch Prepack72162-2425
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-2054
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralREMEDYREPACK INC.70518-4229
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3610
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralNorthwind Health Company, LLC51655-490
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-519
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralSt. Mary's Medical Park Pharmacy60760-676
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralRedpharm Drug67296-2135
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralST. MARY'S MEDICAL PARK PHARMACY60760-689
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-690
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-2097
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-3901

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