NDC codes

FDA NDC Directory
Product NDC (as listed)60505-2522Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60505-2522Add 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
60505-2522-16050525220160 TABLET in 1 BOTTLE (60505-2522-1)Marketed from Oct 18, 2011
60505-2522-36050525220330 TABLET in 1 BOTTLE (60505-2522-3)Marketed from Oct 18, 2011
60505-2522-8605052522081000 TABLET in 1 BOTTLE (60505-2522-8)Marketed from Oct 18, 2011

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)
cilostazol
Generic name (nonproprietary)
cilostazol
Active ingredients
Cilostazol — 100 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077030
Marketing start
Listing expires
Other FDA classes
Phosphodiesterase 3 Inhibitors (Mechanism)
Identifiers
Product ID 60505-2522_a10eb847-1c2f-7cdf-4274-81e6e3aab180SPL ID a10eb847-1c2f-7cdf-4274-81e6e3aab180SPL set ID ceac1ae3-c343-28ca-c083-b748d21a15e6RxCUI 242461, 242462UNII N7Z035406BUPC 0360505252213
Pharmacologic class
Phosphodiesterase 3 Inhibitor

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

N460505252201 followed by a unit qualifier and the quantity

Package 60505-2522-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Cilostazol tablets are indicated for the reduction of symptoms of intermittent claudication, as demonstrated by an increased walking distance. Cilostazol is a phosphodiesterase III inhibitor (PDE III inhibitor) indicated for the reduction of symptoms of intermittent claudication, as demonstrated by an increased walking distance ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077030

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

FDA NDC Directory listings under ANDA 077030
ProductStrengthForm · routeLabelerProduct NDC
cilostazolCilostazol 50 mg/1TabletOralApotex Corp.60505-2521
cilostazolCilostazol 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-813
cilostazolCilostazol 100 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-822
cilostazolCilostazol 100 mg/1TabletOralAvKARE42291-453
cilostazolCilostazol 50 mg/1TabletOralAvPAK50268-176
cilostazolCilostazol 100 mg/1TabletOralAvPAK50268-177

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