What is NDC 24338-550?

24338-550 is the product NDC for Suflave kit, listed with the FDA by Azurity Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Suflave (Polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution).

Azurity Pharmaceuticals, Inc., NDC labeler code 24338. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Suflave?

1 other product NDC are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Suflave NDC 24338-550 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)24338-550Labeler and product segments. Claims need a package NDC.

Product NDC at billing width24338-0550Add 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
24338-550-01	2433805500124338055001	1 KIT in 1 KIT (24338-550-01)Marketed from Apr 1, 2026

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): Suflave
Generic name (nonproprietary): polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution
Dosage form: Kit
Labeler: Azurity Pharmaceuticals, Inc.NDC labeler code 24338
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 215344
Marketing start: Apr 1, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 24338-550_d5710a04-2b0a-402c-a8b0-025766f1a437SPL ID d5710a04-2b0a-402c-a8b0-025766f1a437SPL set ID d5710a04-2b0a-402c-a8b0-025766f1a437RxCUI 2641142, 2641143, 2641144

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N424338055001 followed by a unit qualifier and the quantity

Package 24338-0550-01. 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 Jan 31, 2026.

Indications (excerpt from the label)

SUFLAVE is indicated for the cleansing of the colon as a preparation for colonoscopy in adults. SUFLAVE is an osmotic laxative indicated for cleansing of the colon in preparation for colonoscopy in adults.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24338-550

What is NDC 24338-550?: 24338-550 is the product NDC for Suflave kit, listed with the FDA by Azurity Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Suflave (Polyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution).
Who is the labeler?: Azurity Pharmaceuticals, Inc., NDC labeler code 24338. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Suflave?: 1 other product NDC are listed under this name. See all Suflave 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 Suflave NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Suflavepolyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution	—	Kit	Braintree Laboratories, Inc.	52268-550	52268-0550-01

Other NDCs under NDA 215344

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

FDA NDC Directory listings under NDA 215344
Product	Strength	Form · route	Labeler	Product NDC
Suflavepolyethylene glycol 3350, sodium sulfate, potassium chloride, magnesium sulfate, and sodium chloride for oral solution	—	Kit	Braintree Laboratories, Inc.	52268-550