What is NDC 82868-102?

82868-102 is the product NDC for ciprofloxacin, Ciprofloxacin hydrochloride 250 mg/1 tablet, film coated, listed with the FDA by Northwind Health Company, LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.

Northwind Health Company, LLC, NDC labeler code 82868. 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?

167 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 82868-102 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)82868-102Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82868-0102Add 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
82868-102-06	8286801020682868010206	6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-102-06)Marketed from Oct 8, 2026
82868-102-14	8286801021482868010214	14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-102-14)Marketed from Feb 12, 2026
82868-102-20	8286801022082868010220	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-102-20)Marketed from Jul 21, 2026

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, Film coated
Route: Oral
Labeler: Northwind Health Company, LLCNDC labeler code 82868
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076639
Marketing start: Feb 12, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Cytochrome P450 1A2 Inhibitors (Mechanism)Fluoroquinolones (Chemical structure)
Identifiers: Product ID 82868-102_5d6a3ca6-1c4a-9b13-e063-6394a90aed5cSPL ID 5d6a3ca6-1c4a-9b13-e063-6394a90aed5c
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

N482868010206 followed by a unit qualifier and the quantity

Package 82868-0102-06. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 82868-102

What is NDC 82868-102?: 82868-102 is the product NDC for ciprofloxacin, Ciprofloxacin hydrochloride 250 mg/1 tablet, film coated, listed with the FDA by Northwind Health Company, LLC. It has 3 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?: Northwind Health Company, LLC, NDC labeler code 82868. 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?: 167 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 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	Redpharm Drug	67296-2291	67296-2291-04
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 250 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-976	59651-0976-0159651-0976-2059651-0976-30+1 more
Ciprofloxacinciprofloxacin hydrochloride	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-977	59651-0977-0159651-0977-0559651-0977-20+2 more

All 168 ciprofloxacin NDCs

Other NDCs under ANDA 076639

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

FDA NDC Directory listings under ANDA 076639
Product	Strength	Form · route	Labeler	Product NDC
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-0193
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-767
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	TabletOral	Umasuto, LLC	85293-004
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Umasuto, LLC	85293-002
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Umasuto, LLC	85293-003
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Proficient Rx LP	63187-017
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	QPharma, Inc.	42708-192
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	A-S Medication Solutions	50090-1648
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	A-S Medication Solutions	50090-1649
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4122
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-869
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Bryant Ranch Prepack	71335-0070
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4260
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Proficient Rx LP	63187-142
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-716
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	16571-413
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	16571-411
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	16571-412
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-919
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	TabletOral	Proficient Rx LP	63187-990

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