NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1678Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1678Add 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
70771-1678-170771167801100 CAPSULE in 1 BOTTLE (70771-1678-1)Marketed from Sep 12, 2022
70771-1678-77077116780728 CAPSULE in 1 BOTTLE (70771-1678-7)Marketed from Sep 12, 2022

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 — 10 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 210154
Marketing start
Listing expires
Identifiers
Product ID 70771-1678_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

N470771167801 followed by a unit qualifier and the quantity

Package 70771-1678-01. 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)

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 20 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1034
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 25 mg/1CapsuleOralZydus Pharmaceuticals USA Inc.70710-1035
LenalidomideLenalidomide 2.5 mg/1CapsuleOralZydus Lifesciences Limited70771-1676
LenalidomideLenalidomide 5 mg/1CapsuleOralZydus Lifesciences Limited70771-1677
LenalidomideLenalidomide 25 mg/1CapsuleOralZydus Lifesciences Limited70771-1681
LenalidomideLenalidomide 15 mg/1CapsuleOralZydus Lifesciences Limited70771-1679
LenalidomideLenalidomide 20 mg/1CapsuleOralZydus Lifesciences Limited70771-1680

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