Aprepitant NDC 0781-2322

NDC codes

FDA NDC Directory

Product NDC (as listed)0781-2322Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00781-2322Add 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	Copy
0781-2322-46	00781232246	2 CAPSULE in 1 DOSE PACK (0781-2322-46)Marketed from Dec 27, 2016
0781-2322-68	00781232268	1 BLISTER PACK in 1 CARTON (0781-2322-68) / 6 CAPSULE in 1 BLISTER PACK (0781-2322-06)Marketed from Dec 27, 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): Aprepitant
Generic name (nonproprietary): aprepitant
Active ingredients: Aprepitant — 80 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Sandoz Inc
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 090999
Marketing start: Dec 27, 2016
Listing expires: Dec 31, 2026
Other FDA classes: Cytochrome P450 2C9 Inducers (Mechanism)Cytochrome P450 3A4 Inducers (Mechanism)Cytochrome P450 3A4 Inhibitors (Mechanism)Neurokinin 1 Antagonists (Mechanism)
Identifiers: Product ID 0781-2322_a194823e-5961-4bc0-b18f-2f63d3cbb9c6SPL ID a194823e-5961-4bc0-b18f-2f63d3cbb9c6SPL set ID f58b8944-93ee-4be1-a238-cc0061ddd93aRxCUI 403810, 403811, 644088, 754508UNII 1NF15YR6UY
Pharmacologic class: Substance P/Neurokinin-1 Receptor Antagonist

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

N400781232246 followed by a unit qualifier and the quantity

Package 00781-2322-46. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 090999

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

FDA NDC Directory listings under ANDA 090999
Product	Strength	Form · route	Labeler	Product NDC
Aprepitant	—	Kit	Sandoz Inc	0781-4063
Aprepitant	Aprepitant 40 mg/1	CapsuleOral	Sandoz Inc	0781-2321
Aprepitant	Aprepitant 125 mg/1	CapsuleOral	Sandoz Inc	0781-2323