NDC codes

FDA NDC Directory
Product NDC (as listed)76282-696Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76282-0696Add 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
76282-696-487628206964828 CAPSULE in 1 BOTTLE (76282-696-48)Marketed from Jun 10, 2024

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)
Lenalidomide
Generic name (nonproprietary)
lenalidomide
Active ingredients
Lenalidomide — 2.5 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214618
Marketing start
Listing expires
Identifiers
Product ID 76282-696_ecb5abfb-3a17-4235-a7fe-0183c5586738SPL ID ecb5abfb-3a17-4235-a7fe-0183c5586738SPL set ID 85f5db5d-8f76-46f6-b975-6acda8c4b2c8RxCUI 1242231UNII F0P408N6V4
Pharmacologic class
Thalidomide Analog

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

N476282069648 followed by a unit qualifier and the quantity

Package 76282-0696-48. 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)

Lenalidomide is a thalidomide analogue indicated for the treatment of adult patients with: Multiple myeloma (MM), in combination with dexamethasone (1.1). MM, as maintenance following autologous hematopoietic stem cell transplantation (auto-HSCT) (1.1). Transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes (MDS) associated with a deletion 5q abnormality with or without additional cytogenetic abnormalities (1.2). Mantle cell lymphoma (MCL) whose disease has relapsed or progressed after two prior therapies, one of which included bortezomib (1.3). Previously treated follicular lymphoma (FL), in combination with a rituximab product (1.4). Previously treated ma…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 214618

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

FDA NDC Directory listings under ANDA 214618
ProductStrengthForm · routeLabelerProduct NDC
LenalidomideLenalidomide 2.5 mg/1CapsuleOralCipla USA Inc.69097-604

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