NDC codes

FDA NDC Directory
Product NDC (as listed)71335-1152Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-1152Add 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
71335-1152-0713351152007 TABLET, COATED in 1 BOTTLE (71335-1152-0)Marketed from Jan 29, 2025
71335-1152-17133511520120 TABLET, COATED in 1 BOTTLE (71335-1152-1)Marketed from Jan 29, 2025
71335-1152-27133511520210 TABLET, COATED in 1 BOTTLE (71335-1152-2)Marketed from Jan 29, 2025
71335-1152-37133511520314 TABLET, COATED in 1 BOTTLE (71335-1152-3)Marketed from Jan 29, 2025
71335-1152-4713351152046 TABLET, COATED in 1 BOTTLE (71335-1152-4)Marketed from Jan 29, 2025
71335-1152-57133511520530 TABLET, COATED in 1 BOTTLE (71335-1152-5)Marketed from Jan 29, 2025
71335-1152-67133511520660 TABLET, COATED in 1 BOTTLE (71335-1152-6)Marketed from Jan 29, 2025
71335-1152-77133511520712 TABLET, COATED in 1 BOTTLE (71335-1152-7)Marketed from Jan 29, 2025
71335-1152-87133511520840 TABLET, COATED in 1 BOTTLE (71335-1152-8)Marketed from Jan 29, 2025
71335-1152-97133511520990 TABLET, COATED in 1 BOTTLE (71335-1152-9)Marketed from Jan 29, 2025

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 tablets
Active ingredients
Ciprofloxacin hydrochloride — 250 mg/1
Dosage form
Tablet, Coated
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 71335
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 71335-1152_3bc30d61-cfc5-4855-834d-d82b9f9e040aSPL ID 3bc30d61-cfc5-4855-834d-d82b9f9e040aSPL set ID 8d6ec3ee-2205-4d78-bc48-d39f371797c1RxCUI 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

N471335115200 followed by a unit qualifier and the quantity

Package 71335-1152-00. 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)

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 Exacerbation…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71335-1152

What is NDC 71335-1152?
71335-1152 is the product NDC for Ciprofloxacin (ciprofloxacin tablets), Ciprofloxacin hydrochloride 250 mg/1 tablet, coated, listed with the FDA by Bryant Ranch Prepack. It has 10 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ciprofloxacin (Ciprofloxacin Tablets).
What is the active ingredient?
Ciprofloxacin hydrochloride.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 71335. 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?
168 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 750 mg/1Tablet, Film coatedOralAurobindo Pharma Limited59651-97859651-0978-0159651-0978-0559651-0978-20+2 more

All 169 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 250 mg/1Tablet, CoatedOralPreferred Pharmaceuticals Inc.68788-8200
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralBryant Ranch Prepack71335-2450
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralCoupler LLC67046-1537
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8875
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3693
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralNuCare Pharmaceutical, Inc.68071-3699
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralProficient Rx LP82804-256
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralSolco Healthcare US, LLC43547-689
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralSolco Healthcare US, LLC43547-688
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-2383
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-2384
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralNuCare Pharmaceutical, Inc.68071-3737
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralBryant Ranch Prepack71335-2502
CiprofloxacinCiprofloxacin hydrochloride 250 mg/1Tablet, CoatedOralProficient Rx LP71205-749
CiprofloxacinCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-2404
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralSportpharm LLC85766-099
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralSportpharm LLC85766-100
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 250 mg/1TabletOralREMEDYREPACK INC.70518-4133
CiprofloxacinciprofolxacinCiprofloxacin hydrochloride 500 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8692
Ciprofloxacinciprofloxacin tabletsCiprofloxacin hydrochloride 500 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-1229

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