NDC codes

FDA NDC Directory
Product NDC (as listed)0115-1752Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00115-1752Add 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
0115-1752-080011517520830 CAPSULE in 1 BOTTLE, PLASTIC (0115-1752-08)Marketed from Jan 4, 2016

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Acitretin
Generic name (nonproprietary)
acitretin
Active ingredients
Acitretin — 22.5 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202552
Marketing start
Listing expires
Other FDA classes
Retinoids (Chemical structure)
Identifiers
Product ID 0115-1752_233bc68a-a24e-4f19-8477-3a11e80e68dfSPL ID 233bc68a-a24e-4f19-8477-3a11e80e68dfSPL set ID 85507f6c-f802-479e-bacc-624b5136d092RxCUI 199689, 199690, 894859, 894863UNII LCH760E9T7UPC 0301151753082, 0301151752085
Pharmacologic class
Retinoid

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

N400115175208 followed by a unit qualifier and the quantity

Package 00115-1752-08. 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

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