NDC codes

FDA NDC Directory
Product NDC (as listed)87628-101Labeler and product segments. Claims need a package NDC.
Product NDC at billing width87628-0101Add 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
87628-101-02876280101022 TABLET in 1 BLISTER PACK (87628-101-02)Marketed from Sep 8, 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)
Varubi
Generic name (nonproprietary)
rolapitant
Active ingredients
Rolapitant hydrochloride — 90 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Luria Therapeutics LLCNDC labeler code 87628
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 206500
Marketing start
Listing expires
Other FDA classes
Breast Cancer Resistance Protein Inhibitors (Mechanism)Cytochrome P450 2D6 Inhibitors (Mechanism)Neurokinin 1 Antagonists (Mechanism)P-Glycoprotein Inhibitors (Mechanism)
Identifiers
Product ID 87628-101_25c6e790-1e90-4901-b85b-f24d2c8c2b04SPL ID 25c6e790-1e90-4901-b85b-f24d2c8c2b04SPL set ID 8670c3cf-82d9-466d-be49-de33d8c8742bRxCUI 1665503, 1673373UNII 57O5S1QSAQ
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

N487628010102 followed by a unit qualifier and the quantity

Package 87628-0101-02. 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)

VARUBI ® is indicated in combination with other antiemetic agents in adults for the prevention of delayed nausea and vomiting associated with initial and repeat courses of emetogenic cancer chemotherapy, including, but not limited to, highly emetogenic chemotherapy. VARUBI is a substance P/neurokinin 1 (NK1) receptor antagonist indicated in combination with other antiemetic agents in adults for the prevention of delayed nausea and vomiting associated with initial and repeat courses of emetogenic cancer chemotherapy, including, but not limited to, highly emetogenic chemotherapy. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 87628-101

What is NDC 87628-101?
87628-101 is the product NDC for Varubi (rolapitant), Rolapitant hydrochloride 90 mg/1 tablet, listed with the FDA by Luria Therapeutics LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Varubi (Rolapitant).
What is the active ingredient?
Rolapitant hydrochloride.
Who is the labeler?
Luria Therapeutics LLC, NDC labeler code 87628. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Varubi?
1 other product NDC are listed under this name. See all Varubi 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 Varubi NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
VarubirolapitantRolapitant hydrochloride 90 mg/1TabletOralTerSera Therapeutics LLC70720-10170720-0101-02

Other NDCs under NDA 206500

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

FDA NDC Directory listings under NDA 206500
ProductStrengthForm · routeLabelerProduct NDC
VarubirolapitantRolapitant hydrochloride 90 mg/1TabletOralTerSera Therapeutics LLC70720-101

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