NDC codes

FDA NDC Directory
Product NDC (as listed)68462-585Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68462-0585Add 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
68462-585-76684620585761 BLISTER PACK in 1 CARTON (68462-585-76) / 6 CAPSULE in 1 BLISTER PACK (68462-585-40)Marketed from Oct 12, 2017

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
Active ingredients
Aprepitant — 125 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Glenmark Pharmaceuticals Inc., USANDC labeler code 68462
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207777
Marketing start
Listing expires
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 68462-585_41f97256-ac39-413d-8b2f-5fb7ad429143SPL ID 41f97256-ac39-413d-8b2f-5fb7ad429143SPL set ID d72e0e10-4557-41b0-b65d-d395468cad19RxCUI 403810, 403811, 644088, 754508UNII 1NF15YR6UYUPC 0368462585764, 0368462112335, 0368462584767, 0368462583401
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

N468462058576 followed by a unit qualifier and the quantity

Package 68462-0585-76. 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 .

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 ) o 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. • Chroni…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68462-585

What is NDC 68462-585?
68462-585 is the product NDC for Aprepitant, Aprepitant 125 mg/1 capsule, listed with the FDA by Glenmark Pharmaceuticals Inc., USA. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Aprepitant.
What is the active ingredient?
Aprepitant.
Who is the labeler?
Glenmark Pharmaceuticals Inc., USA, NDC labeler code 68462. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
AprepitantAprepitant 125 mg/1CapsuleOralBluePoint Laboratories68001-66868001-0668-19
Aprepitant—KitBluePoint Laboratories68001-66968001-0669-15
AprepitantAprepitant 40 mg/1CapsuleOralBluePoint Laboratories68001-66668001-0666-0168001-0666-17
AprepitantAprepitant 80 mg/1CapsuleOralBluePoint Laboratories68001-66768001-0667-0168001-0667-19
AprepitantAprepitant 40 mg/1CapsuleOralGolden State Medical Supply, Inc.51407-70151407-0701-0151407-0701-05
AprepitantAprepitant 80 mg/1CapsuleOralGolden State Medical Supply, Inc.51407-70251407-0702-0251407-0702-06
AprepitantAprepitant 125 mg/1CapsuleOralGolden State Medical Supply, Inc.51407-70351407-0703-06
Aprepitant—KitGolden State Medical Supply, Inc.51407-70451407-0704-03
AprepitantAprepitant 40 mg/1CapsuleOralTorrent Pharmaceuticals Limited13668-59113668-0591-8113668-0591-82
AprepitantAprepitant 80 mg/1CapsuleOralTorrent Pharmaceuticals Limited13668-59213668-0592-8413668-0592-86

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
ProductStrengthForm · routeLabelerProduct NDC
AprepitantAprepitant 40 mg/1CapsuleOralBluePoint Laboratories68001-666
Aprepitant—KitBluePoint Laboratories68001-669
AprepitantAprepitant 80 mg/1CapsuleOralBluePoint Laboratories68001-667
AprepitantAprepitant 125 mg/1CapsuleOralBluePoint Laboratories68001-668
AprepitantAprepitant 40 mg/1CapsuleOralGlenmark Pharmaceuticals Inc., USA68462-583
AprepitantAprepitant 80 mg/1CapsuleOralGlenmark Pharmaceuticals Inc., USA68462-584
Aprepitant—KitGlenmark Pharmaceuticals Inc., USA68462-112

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Aprepitant NDC 68462-585 | National Drug Code | Med-Code