NDC codes

FDA NDC Directory
Product NDC (as listed)81033-241Labeler and product segments. Claims need a package NDC.
Product NDC at billing width81033-0241Add 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
81033-241-328103302413281033024132946 mL in 1 BOTTLE, PLASTIC (81033-241-32)Marketed from Feb 2, 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 Solution
Generic name (nonproprietary)
lactulose solution usp, 10 g/15 ml
Active ingredients
Lactulose — 10 g/15mL
Dosage form
Solution
Route
Oral, Rectal
Labeler
Kesin Pharma CorporationNDC labeler code 81033
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076645
Marketing start
Listing expires
Other FDA classes
Acidifying Activity (Mechanism)Osmotic Activity (Mechanism)Stimulation Large Intestine Fluid/Electrolyte Secretion (Physiologic effect)
Identifiers
Product ID 81033-241_5825ed21-67c0-40d9-e063-6294a90a8103SPL ID 5825ed21-67c0-40d9-e063-6294a90a8103SPL set ID 2d90e2a4-334f-ab68-e063-6294a90affa6RxCUI 391937UNII 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 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

N481033024132 followed by a unit qualifier and the quantity

Package 81033-0241-32. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE For the prevention and treatment of portal-systemic encephalopathy, including the stages of hepatic pre-coma and coma. Controlled studies have shown that lactulose solution therapy reduces the blood ammonia level by 25 to 50%; this is generally paralleled by an improvement in the patients’ mental state and by an improvement in EEG patterns. The clinical response has been observed in about 75% of patients, which is at least as satisfactory as that resulting from neomycin therapy. An increase in patients’ protein tolerance is also frequently observed with lactulose solution therapy. In the treatment of chronic portal-systemic encephalopathy, lactulose solution has been gi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 81033-241

What is NDC 81033-241?
81033-241 is the product NDC for Lactulose Solution, Lactulose 10 g/15mL solution, listed with the FDA by Kesin Pharma Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lactulose Solution (Lactulose Solution USP, 10 g/15 mL).
What is the active ingredient?
Lactulose.
Who is the labeler?
Kesin Pharma Corporation, NDC labeler code 81033. 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 Solution?
2 other product NDCs are listed under this name. See all Lactulose Solution 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 Solution NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Lactulose Solutionlactulose solution usp, 10 g/15 mlLactulose 10 g/15mLSolutionOral, RectalBajaj Medical, LLC61037-47161037-0471-0261037-0471-0361037-0471-04+5 more
Lactulose Solutionlactulose solution usp, 10 g/15 mlLactulose 10 g/15mLSolutionOral, RectalRising Pharma Holdings, Inc.64980-59264980-0592-1264980-0592-2464980-0592-48+1 more

Other NDCs under ANDA 076645

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

FDA NDC Directory listings under ANDA 076645
ProductStrengthForm · routeLabelerProduct NDC
Lactulose Solutionlactulose solution usp, 10 g/15 mlLactulose 10 g/15mLSolutionOral, RectalBajaj Medical, LLC61037-471
Lactulose Solutionlactulose solution usp, 10 g/15 mlLactulose 10 g/15mLSolutionOral, RectalRising Pharma Holdings, Inc.64980-592

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