NDC codes

FDA NDC Directory
Product NDC (as listed)60505-4744Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60505-4744Add 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
60505-4744-160505474401100 CAPSULE in 1 BOTTLE (60505-4744-1)Marketed from Nov 9, 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)
Lisdexamfetamine Dimesylate
Generic name (nonproprietary)
lisdexamfetamine dimesylate
Active ingredients
Lisdexamfetamine dimesylate — 60 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216944
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)
Identifiers
Product ID 60505-4744_0190bec9-05e4-0977-9548-2cc150b53e74SPL ID 0190bec9-05e4-0977-9548-2cc150b53e74

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

N460505474401 followed by a unit qualifier and the quantity

Package 60505-4744-01. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 216944

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

FDA NDC Directory listings under ANDA 216944
ProductStrengthForm · routeLabelerProduct NDC
Lisdexamfetamine DimesylateLisdexamfetamine dimesylate 40 mg/1CapsuleOralApotex Corp.60505-4742
Lisdexamfetamine DimesylateLisdexamfetamine dimesylate 10 mg/1CapsuleOralApotex Corp.60505-4739
Lisdexamfetamine DimesylateLisdexamfetamine dimesylate 20 mg/1CapsuleOralApotex Corp.60505-4740
Lisdexamfetamine DimesylateLisdexamfetamine dimesylate 30 mg/1CapsuleOralApotex Corp.60505-4741
Lisdexamfetamine DimesylateLisdexamfetamine dimesylate 50 mg/1CapsuleOralApotex Corp.60505-4743
Lisdexamfetamine DimesylateLisdexamfetamine dimesylate 70 mg/1CapsuleOralApotex Corp.60505-4745

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Lisdexamfetamine Dimesylate NDC 60505-4744 | Med-Code