What is NDC 63187-142?

63187-142 is the product NDC for ciprofloxacin, Ciprofloxacin hydrochloride 250 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 8 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 63187. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

ciprofloxacin NDC 63187-142 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63187-142Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63187-0142Add 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
63187-142-06	63187014206	6 TABLET in 1 BOTTLE (63187-142-06)Marketed from Aug 1, 2014
63187-142-10	63187014210	10 TABLET in 1 BOTTLE (63187-142-10)Marketed from Aug 1, 2014
63187-142-14	63187014214	14 TABLET in 1 BOTTLE (63187-142-14)Marketed from Aug 1, 2014
63187-142-20	63187014220	20 TABLET in 1 BOTTLE (63187-142-20)Marketed from Aug 1, 2014
63187-142-28	63187014228	28 TABLET in 1 BOTTLE (63187-142-28)Marketed from Aug 1, 2014
63187-142-30	63187014230	30 TABLET in 1 BOTTLE (63187-142-30)Marketed from Jul 23, 2021
63187-142-60	63187014260	60 TABLET in 1 BOTTLE (63187-142-60)Marketed from Jul 23, 2021
63187-142-90	63187014290	90 TABLET in 1 BOTTLE (63187-142-90)Marketed from Jul 23, 2021

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: Proficient Rx LPNDC labeler code 63187
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076639
Marketing start: Sep 10, 2004
Listing expires: Dec 31, 2026
Other FDA classes: Quinolones (Chemical structure)
Identifiers: Product ID 63187-142_91f426fc-3fc4-4c2f-a56d-10862e54d745SPL ID 91f426fc-3fc4-4c2f-a56d-10862e54d745SPL set ID fbcd32c0-bcfd-4cc7-8e81-6612bc0cfc45RxCUI 197511, 309309UNII 4BA73M5E37UPC 0363187142100, 0363187017101
Pharmacologic class: Quinolone Antimicrobial

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

N463187014206 followed by a unit qualifier and the quantity

Package 63187-0142-06. 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 Jun 1, 2022. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Ciprofloxacin Tablets USP, 250 mg and 500 mg is indicated for the treatment of infections caused by susceptible strains of the designated microorganisms in the conditions and patient populations listed below. Please see Error! Hyperlink reference not valid. for specific recommendations. Adult Patients: Urinary Tract Infections caused by Escherichia coli, Klebsiella pneumoniae, Enterobacter cloacae, Serratia marcescens, Proteus mirabilis, Providencia rettgeri, Morganella morganii, Citrobacter diversus, Citrobacter freundii, Pseudomonas aeruginosa, methicillin-susceptible Staphylococcus epidermidis, Staphylococcus saprophyticus, or Enterococcus faecalis. Acute Uncomplicat…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63187-142

What is NDC 63187-142?: 63187-142 is the product NDC for ciprofloxacin, Ciprofloxacin hydrochloride 250 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 8 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?: Proficient Rx LP, NDC labeler code 63187. 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
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 250 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	59651-976	59651-0976-0159651-0976-2059651-0976-30+1 more

All 170 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	TabletOral	A-S Medication Solutions	50090-1648
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-767
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-4260
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-716
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	66267-919
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	TabletOral	Proficient Rx LP	63187-990
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	QPharma, Inc.	42708-192
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-869
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	Umasuto, LLC	85293-003
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	82868-102
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Umasuto, LLC	85293-002
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	TabletOral	Umasuto, LLC	85293-004
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7243
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	Bryant Ranch Prepack	71335-0408
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	TabletOral	Coupler LLC	67046-1528
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	16571-411
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	TabletOral	A-S Medication Solutions	50090-1649
ciprofloxacin	Ciprofloxacin hydrochloride 500 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	16571-412
ciprofloxacin	Ciprofloxacin hydrochloride 750 mg/1	Tablet, Film coatedOral	Rising Pharma Holdings, Inc.	16571-413
ciprofloxacin	Ciprofloxacin hydrochloride 250 mg/1	TabletOral	PharmPak, Inc.	54348-662

Showing 20 of 26.