What is the correct format for NDC numbers?

Proper billing of a National Drug Code (NDC) requires an 11-digit number in a 5-4-2 format.

How do I find my NDC Product code?

You can also access NDC numbers via the free Drugs.com Medication Guide App. The FDA also maintains a searchable database of NDC codes on their website. NDC numbers can also be found in the drug product labeling (for example, the package insert) as well as on the package itself.

What is the NDC for triamcinolone acetonide?

Kenalog®-80 Injection (triamcinolone acetonide injectable suspension, USP) is supplied in vials providing 80 mg triamcinolone acetonide per mL….LOCAL.

40 mg/mL, 1 mL vial	NDC 0003-0293-05
40 mg/mL, 10 mL vial	NDC 0003-0293-28

What does the 3 sets of numbers on the NDC number mean?

The code is present on all nonprescription (OTC) and prescription medication packages and inserts in the US. The 3 segments of the NDC identify the labeler, the product, and the commercial package size. The first set of numbers in the NDC identifies the labeler (manufacturer, repackager, or distributer).

What is the difference between NDC and UPC?

Each NDC-coded product package in the US bears a barcode with a Universal Product Code that begins with a 3 (UPC-A) or 03 (EAN-13). If the NDC is used in the UPC it is the most minimal form of the NDC code with 10 digits only.

What is a deprecated NDC code?

Deprecated in NDC means they are no longer active codes used by the manufacturer.

What is procedure code J3301?

The descriptor for J3301 is Injection, triamcinolone acetonide, not otherwise specified, 10 mg.

What is the NDC code for J3301?

KENALOG 40MG/ML 10ML VL EACH

Package AWP:	$82.43
J-Code:	J3301 Injection, triamcinolone acetonide, not otherwise specified, 10 mg
Strength:	40 MG/1 ML
Form:	Suspension
NDC Number:	00003029328 00003-0293-28

What do the first 5 digits of an NDC number represent?

The National Drug Code (NDC) is the number which identifies a drug. The first 5 digits identify the labeler code representing the manufacturer of the drug and are assigned by the Food and Drug Administration (FDA). ▪ The next 4 digits identify the specific drug product and are assigned by the manufacturer.