NDC codes

FDA NDC Directory
Product NDC (as listed)69557-333Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69557-0333Add 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
69557-333-0169557033301695570333016 BOTTLE in 1 CARTON (69557-333-01) / 4.8 mL in 1 BOTTLEMarketed from Nov 27, 2023
69557-333-0269557033302695570333021 BOTTLE in 1 CARTON (69557-333-02) / 4.8 mL in 1 BOTTLEMarketed from Nov 27, 2023 · Sample package

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)
ELYXYB - celecoxib
Generic name (nonproprietary)
celecoxib
Active ingredients
Celecoxib — 120 mg/4.8mL
Dosage form
Liquid
Route
Oral
Labeler
SCILEX PHARMACEUTICALS INC.NDC labeler code 69557
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 212157
Marketing start
Listing expires
Other FDA classes
Non-Steroidal (Chemical structure)Cyclooxygenase Inhibitors (Mechanism)
Identifiers
Product ID 69557-333_ad5c6af3-1790-4a13-b4e5-6e3af543b2a8SPL ID ad5c6af3-1790-4a13-b4e5-6e3af543b2a8SPL set ID c8a5de07-9f27-4a54-a885-8089f0307bd7RxCUI 2373454, 2373460UNII JCX84Q7J1L

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

N469557033301 followed by a unit qualifier and the quantity

Package 69557-0333-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

ELYXYB is indicated for the acute treatment of migraine with or without aura in adults. Limitations of Use ELYXYB is not indicated for the preventive treatment of migraine. ELYXYB is a nonsteroidal anti-inflammatory drug indicated for the acute treatment of migraine with or without aura in adults ( 1 ) Limitations of Use ELYXYB is not indicated for the preventive treatment of migraine. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 69557-333

What is NDC 69557-333?
69557-333 is the product NDC for ELYXYB - celecoxib (celecoxib), Celecoxib 120 mg/4.8mL liquid, listed with the FDA by SCILEX PHARMACEUTICALS INC.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
ELYXYB - celecoxib (Celecoxib).
What is the active ingredient?
Celecoxib.
Who is the labeler?
SCILEX PHARMACEUTICALS INC., NDC labeler code 69557. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for ELYXYB - celecoxib?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in