What is NDC 73352-900?

73352-900 is the product NDC for Lactulose, Lactulose 10 g/10g powder, for solution, listed with the FDA by Trifluent Pharma, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Trifluent Pharma, Inc., NDC labeler code 73352. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Lactulose?

24 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Lactulose NDC 73352-900 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)73352-900Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73352-0900Add 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
73352-900-15	7335209001573352090015	15 POUCH in 1 CARTON (73352-900-15) / 10 g in 1 POUCH (73352-900-01)Marketed from Sep 13, 2025

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): Lactulose
Generic name (nonproprietary): lactulose
Active ingredients: Lactulose — 10 g/10g
Dosage form: Powder, For solution
Route: Oral
Labeler: Trifluent Pharma, Inc.NDC labeler code 73352
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217914
Marketing start: Sep 13, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Acidifying Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers: Product ID 73352-900_3eaf2342-fb58-e0a5-e063-6394a90a7271SPL ID 3eaf2342-fb58-e0a5-e063-6394a90a7271SPL set ID 3eaf273a-b49d-2595-e063-6394a90a1cf6RxCUI 1251190, 1251194UNII 9U7D5QH5AE
Pharmacologic class: Osmotic Laxative

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

N473352090015 followed by a unit qualifier and the quantity

Package 73352-0900-15. 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 Sep 13, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE Lactulose for Oral Solution is indicated for the treatment of constipation. In patients with a history of chronic constipation, lactulose therapy increases the number of bowel movements per day and the number of days on which bowel movements occur.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 73352-900

What is NDC 73352-900?: 73352-900 is the product NDC for Lactulose, Lactulose 10 g/10g powder, for solution, listed with the FDA by Trifluent Pharma, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Lactulose.
What is the active ingredient?: Lactulose.
Who is the labeler?: Trifluent Pharma, Inc., NDC labeler code 73352. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lactulose?: 24 other product NDCs are listed under this name. See all Lactulose 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 Lactulose NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Lactulose	Lactulose 10 g/15mL	SolutionOral	American Health Packaging	60687-917	60687-0917-1460687-0917-6460687-0917-76
Lactulose	Lactulose 20 g/20g	Powder, For solutionOral	Trifluent Pharma, Inc.	73352-905	73352-0905-15
Lactulose	Lactulose 10 g/15mL	SolutionOral	Sun Pharmaceutical Industries, Inc.	51672-4243	51672-4243-09
Lactulose	Lactulose 10 g/10g	Powder, For solutionOral	PAI Holdings, LLC dba PAI Pharma	0121-0965	00121-0965-30
Lactulose	Lactulose 20 g/20g	Powder, For solutionOral	PAI Holdings, LLC dba PAI Pharma	0121-1930	00121-1930-30
Lactulose	Lactulose 20 g/20g	SolutionOral	Foxland Pharmaceuticals, Inc.	69067-020	69067-0020-15
Lactulose	Lactulose 10 g/15mL	SolutionOral, Rectal	APOZEAL PHARMACEUTICALS INC	83745-249	83745-0249-0883745-0249-1683745-0249-32
Lactulose	Lactulose 10 g/15mL	SolutionOral	APOZEAL PHARMACEUTICALS INC	83745-405	83745-0405-1683745-0405-32
Lactulose	Lactulose 10 g/15mL	SolutionOral	Xttrium Laboratories, Inc.	0116-4005	00116-4005-0800116-4005-1000116-4005-11+4 more
Lactulose	Lactulose 10 g/15mL	SolutionOral	PAI Holdings, LLC dba PAI Pharma	0121-0873	00121-0873-1500121-0873-1600121-0873-32

All 25 Lactulose NDCs

Other NDCs under ANDA 217914

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

FDA NDC Directory listings under ANDA 217914
Product	Strength	Form · route	Labeler	Product NDC
Lactulose	Lactulose 10 g/10g	Powder, For solutionOral	PAI Holdings, LLC dba PAI Pharma	0121-0965
Lactulose	Lactulose 20 g/20g	Powder, For solutionOral	PAI Holdings, LLC dba PAI Pharma	0121-1930
Lactulose	Lactulose 20 g/20g	Powder, For solutionOral	Trifluent Pharma, Inc.	73352-905