NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1676Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1676Add 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
70771-1676-17077116760170771167601100 CAPSULE in 1 BOTTLE (70771-1676-1)Marketed from Mar 7, 2023
70771-1676-7707711676077077116760728 CAPSULE in 1 BOTTLE (70771-1676-7)Marketed from Mar 7, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Labeler
Zydus Lifesciences LimitedNDC labeler code 70771
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210154
Marketing start
Listing expires
Identifiers
Product ID 70771-1676_b85844ee-03a3-407f-97a9-ae0098212923SPL ID b85844ee-03a3-407f-97a9-ae0098212923SPL set ID fd23328f-b019-4c14-80d9-4ebd997f26b2RxCUI 602910, 602912, 643712, 643720, 1242231, 1428947UNII 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

N470771167601 followed by a unit qualifier and the quantity

Package 70771-1676-01. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 70771-1676

What is NDC 70771-1676?
70771-1676 is the product NDC for Lenalidomide, Lenalidomide 2.5 mg/1 capsule, listed with the FDA by Zydus Lifesciences Limited. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lenalidomide.
What is the active ingredient?
Lenalidomide.
Who is the labeler?
Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lenalidomide?
107 other product NDCs are listed under this name. See all Lenalidomide 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 Lenalidomide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LenalidomideLenalidomide 2.5 mg/1CapsuleOralAccord Healthcare Inc.16729-69216729-0692-09
LenalidomideLenalidomide 25 mg/1CapsuleOralAccord Healthcare Inc.16729-69716729-0697-06
LenalidomideLenalidomide 15 mg/1CapsuleOralAccord Healthcare Inc.16729-69516729-0695-06
LenalidomideLenalidomide 5 mg/1CapsuleOralAccord Healthcare Inc.16729-69316729-0693-09
LenalidomideLenalidomide 20 mg/1CapsuleOralAccord Healthcare Inc.16729-69616729-0696-06
LenalidomideLenalidomide 10 mg/1CapsuleOralAccord Healthcare Inc.16729-69416729-0694-09
LenalidomideLenalidomide 2.5 mg/1CapsuleOralPadagis US LLC0574-140200574-1402-28
LenalidomideLenalidomide 5 mg/1CapsuleOralPadagis US LLC0574-140500574-1405-28
LenalidomideLenalidomide 10 mg/1CapsuleOralPadagis US LLC0574-141000574-1410-28
LenalidomideLenalidomide 15 mg/1CapsuleOralPadagis US LLC0574-141500574-1415-21

All 108 Lenalidomide NDCs

Other NDCs under ANDA 210154

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

FDA NDC Directory listings under ANDA 210154
ProductStrengthForm · routeLabelerProduct NDC
LenalidomideLenalidomide 2.5 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1030
LenalidomideLenalidomide 5 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1031
LenalidomideLenalidomide 10 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1032
LenalidomideLenalidomide 15 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1033
LenalidomideLenalidomide 20 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1034
LenalidomideLenalidomide 25 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1035
LenalidomideLenalidomide 5 mg/1CapsuleOralZydus Lifesciences Limited70771-1677
LenalidomideLenalidomide 10 mg/1CapsuleOralZydus Lifesciences Limited70771-1678
LenalidomideLenalidomide 15 mg/1CapsuleOralZydus Lifesciences Limited70771-1679
LenalidomideLenalidomide 20 mg/1CapsuleOralZydus Lifesciences Limited70771-1680
LenalidomideLenalidomide 25 mg/1CapsuleOralZydus Lifesciences Limited70771-1681

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