What is NDC 68001-669?

68001-669 is the product NDC for Aprepitant kit, listed with the FDA by BluePoint Laboratories. It has 1 package NDC, shown above in 10- and 11-digit form.

BluePoint Laboratories, NDC labeler code 68001. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Aprepitant?

19 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Aprepitant NDC 68001-669 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68001-669Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68001-0669Add 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
68001-669-15	68001066915	1 KIT in 1 DOSE PACK (68001-669-15) * 2 CAPSULE in 1 BLISTER PACK * 1 CAPSULE in 1 BLISTER PACKMarketed from Feb 3, 2026

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): Aprepitant
Generic name (nonproprietary): aprepitant
Dosage form: Kit
Labeler: BluePoint LaboratoriesNDC labeler code 68001
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207777
Marketing start: Feb 3, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 68001-669_4e00638d-1cbc-f20f-e063-6294a90ac14cSPL ID 4e00638d-1cbc-f20f-e063-6294a90ac14cSPL set ID a78aaa00-a46b-4f9e-a415-2fca9e9a4fb4RxCUI 403810, 403811, 644088, 754508UNII 1NF15YR6UYUPC 0368001669153

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N468001066915 followed by a unit qualifier and the quantity

Package 68001-0669-15. 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 Mar 27, 2026.

Indications (excerpt from the label)

Aprepitant is a substance P/neurokinin 1 (NK 1 ) receptor antagonist. Aprepitant capsules are indicated in combination with other antiemetic agents, in patients 12 years of age and older for prevention of: acute and delayed nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy (HEC) including high-dose cisplatin ( 1.1 ) nausea and vomiting associated with initial and repeat courses of moderately emetogenic cancer chemotherapy (MEC) ( 1.1 ) for prevention of postoperative nausea and vomiting (PONV) in adults ( 1.2 ) Limitations of Use : ( 1.3 ) Aprepitant has not been studied for treatment of established nausea and vomiting. Chronic continuous…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68001-669

What is NDC 68001-669?: 68001-669 is the product NDC for Aprepitant kit, listed with the FDA by BluePoint Laboratories. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Aprepitant.
Who is the labeler?: BluePoint Laboratories, NDC labeler code 68001. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Aprepitant?: 19 other product NDCs are listed under this name. See all Aprepitant 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 Aprepitant NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Aprepitant	Aprepitant 125 mg/1	CapsuleOral	BluePoint Laboratories	68001-668	68001-0668-19
Aprepitant	Aprepitant 40 mg/1	CapsuleOral	BluePoint Laboratories	68001-666	68001-0666-0168001-0666-17
Aprepitant	Aprepitant 80 mg/1	CapsuleOral	BluePoint Laboratories	68001-667	68001-0667-0168001-0667-19
Aprepitant	—	Kit	Golden State Medical Supply, Inc.	51407-704	51407-0704-03
Aprepitant	Aprepitant 40 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	51407-701	51407-0701-0151407-0701-05
Aprepitant	Aprepitant 80 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	51407-702	51407-0702-0251407-0702-06
Aprepitant	Aprepitant 125 mg/1	CapsuleOral	Golden State Medical Supply, Inc.	51407-703	51407-0703-06
Aprepitant	—	Kit	Torrent Pharmaceuticals Limited	13668-594	13668-0594-87
Aprepitant	Aprepitant 40 mg/1	CapsuleOral	Torrent Pharmaceuticals Limited	13668-591	13668-0591-8113668-0591-82
Aprepitant	Aprepitant 80 mg/1	CapsuleOral	Torrent Pharmaceuticals Limited	13668-592	13668-0592-8413668-0592-86

All 20 Aprepitant NDCs

Other NDCs under ANDA 207777

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

FDA NDC Directory listings under ANDA 207777
Product	Strength	Form · route	Labeler	Product NDC
Aprepitant	Aprepitant 40 mg/1	CapsuleOral	Glenmark Pharmaceuticals Inc., USA	68462-583
Aprepitant	Aprepitant 80 mg/1	CapsuleOral	Glenmark Pharmaceuticals Inc., USA	68462-584
Aprepitant	Aprepitant 125 mg/1	CapsuleOral	Glenmark Pharmaceuticals Inc., USA	68462-585
Aprepitant	—	Kit	Glenmark Pharmaceuticals Inc., USA	68462-112
Aprepitant	Aprepitant 40 mg/1	CapsuleOral	BluePoint Laboratories	68001-666
Aprepitant	Aprepitant 80 mg/1	CapsuleOral	BluePoint Laboratories	68001-667
Aprepitant	Aprepitant 125 mg/1	CapsuleOral	BluePoint Laboratories	68001-668