Lumryz (sodium oxybate) NDC 13551-002

NDC codes

FDA NDC Directory

Product NDC (as listed)13551-002Labeler and product segments. Claims need a package NDC.

Product NDC at billing width13551-0002Add 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 NDC	11-digit (billing)	Package	Copy
13551-002-07	13551000207	7 PACKET in 1 CARTON (13551-002-07) / 1 FOR SUSPENSION, EXTENDED RELEASE in 1 PACKETMarketed from May 1, 2023
13551-002-30	13551000230	30 PACKET in 1 CARTON (13551-002-30) / 1 FOR SUSPENSION, EXTENDED RELEASE in 1 PACKETMarketed from May 1, 2023

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): Lumryz
Generic name (nonproprietary): sodium oxybate
Active ingredients: Sodium oxybate — 6 g/1
Dosage form: For suspension, Extended release
Route: Oral
Labeler: Alkermes, Inc.
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 214755
Marketing start: May 1, 2023
Listing expires: Dec 31, 2027
DEA schedule: CIII
Other FDA classes: Central Nervous System Depression (Physiologic effect)Decreased Central Nervous System Organized Electrical Activity (Physiologic effect)
Identifiers: Product ID 13551-002_0aae7705-0d32-4900-8233-0b3da243bed6SPL ID 0aae7705-0d32-4900-8233-0b3da243bed6
Pharmacologic class: Central Nervous System Depressant

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

N413551000207 followed by a unit qualifier and the quantity

Package 13551-0002-07. 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.