What is NDC 68071-2384?

68071-2384 is the product NDC for Ciprofloxacin, Ciprofloxacin hydrochloride 500 mg/1 tablet, coated, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 9 package NDCs, shown above in 10- and 11-digit form.

NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ciprofloxacin NDC 68071-2384 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68071-2384Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68071-2384Add 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 NDC	11-digit (billing)	Package
68071-2384-1	68071238401	10 TABLET, COATED in 1 BOTTLE (68071-2384-1)Marketed from Apr 9, 2021
68071-2384-2	68071238402	20 TABLET, COATED in 1 BOTTLE (68071-2384-2)Marketed from Apr 9, 2021
68071-2384-3	68071238403	30 TABLET, COATED in 1 BOTTLE (68071-2384-3)Marketed from Apr 9, 2021
68071-2384-4	68071238404	14 TABLET, COATED in 1 BOTTLE (68071-2384-4)Marketed from Apr 9, 2021
68071-2384-5	68071238405	15 TABLET, COATED in 1 BOTTLE (68071-2384-5)Marketed from Apr 9, 2021
68071-2384-6	68071238406	60 TABLET, COATED in 1 BOTTLE (68071-2384-6)Marketed from Apr 9, 2021
68071-2384-7	68071238407	21 TABLET, COATED in 1 BOTTLE (68071-2384-7)Marketed from Apr 9, 2021
68071-2384-8	68071238408	28 TABLET, COATED in 1 BOTTLE (68071-2384-8)Marketed from Apr 9, 2021
68071-2384-9	68071238409	90 TABLET, COATED in 1 BOTTLE (68071-2384-9)Marketed from Apr 9, 2021

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 — 500 mg/1
Dosage form: Tablet, Coated
Route: Oral
Labeler: NuCare Pharmaceuticals,Inc.NDC labeler code 68071
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208921
Marketing start: Aug 12, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 1A2 Inhibitors (Mechanism)Fluoroquinolones (Chemical structure)
Identifiers: Product ID 68071-2384_4c261b8a-4e9d-8f10-e063-6394a90a0ab8SPL ID 4c261b8a-4e9d-8f10-e063-6394a90a0ab8SPL set ID bf8d4359-a850-97b7-e053-2a95a90aa66aRxCUI 309309UNII 4BA73M5E37UPC 0368071238488
Pharmacologic class: Fluoroquinolone Antibacterial

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

N468071238401 followed by a unit qualifier and the quantity

Package 68071-2384-01. 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

Current FDA label (SPL), effective Mar 3, 2026. 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 68071-2384

What is NDC 68071-2384?: 68071-2384 is the product NDC for Ciprofloxacin, Ciprofloxacin hydrochloride 500 mg/1 tablet, coated, listed with the FDA by NuCare Pharmaceuticals,Inc.. It has 9 package NDCs, 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?: NuCare Pharmaceuticals,Inc., NDC labeler code 68071. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-947	60687-0947-01
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	82868-102	82868-0102-1482868-0102-20
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-0193	55154-0193-00
Ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Direct_Rx	72189-627	72189-0627-1072189-0627-14
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8875	68788-8875-0068788-8875-0168788-8875-02+4 more
Ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Direct_Rx	72189-623	72189-0623-1072189-0623-1472189-0623-20
Ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	St. Mary's Medical Park Pharmacy	60760-690	60760-0690-10
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	NCS HealthCare of KY, LLC dba Vangard Labs	0615-8630	00615-8630-1000615-8630-1400615-8630-20
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-977	59651-0977-0159651-0977-0559651-0977-20+2 more
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 750 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-978	59651-0978-0159651-0978-0559651-0978-20+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
Product	Strength	Form · route	Labeler	Product NDC
Ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	Tablet, CoatedOral	Preferred Pharmaceuticals Inc.	68788-8200
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Bryant Ranch Prepack	71335-2450
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Coupler LLC	67046-1537
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8875
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3693
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	NuCare Pharmaceutical, Inc.	68071-3699
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Proficient Rx LP	82804-256
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Solco Healthcare US, LLC	43547-689
Ciprofloxacinciprofloxacin tablets	Ciprofloxacin hydrochloride 250 mg/1	Tablet, CoatedOral	Bryant Ranch Prepack	71335-1152
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Solco Healthcare US, LLC	43547-688
Ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	Tablet, CoatedOral	NuCare Pharmaceuticals,Inc.	68071-2383
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	NuCare Pharmaceutical, Inc.	68071-3737
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Bryant Ranch Prepack	71335-2502
Ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	Tablet, CoatedOral	Proficient Rx LP	71205-749
Ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, CoatedOral	NuCare Pharmaceuticals,Inc.	68071-2404
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Sportpharm LLC	85766-099
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Sportpharm LLC	85766-100
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	REMEDYREPACK INC.	70518-4133
Ciprofloxacinciprofolxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8692
Ciprofloxacinciprofloxacin tablets	Ciprofloxacin hydrochloride 500 mg/1	Tablet, CoatedOral	Bryant Ranch Prepack	71335-1229

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