NDC codes

FDA NDC Directory
Product NDC (as listed)72559-021Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72559-0021Add 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
72559-021-0572559002105725590021051 BOTTLE in 1 CARTON (72559-021-05) / 90 TABLET in 1 BOTTLEMarketed from Jan 24, 2023
72559-021-567255900215672559002156180 TABLET in 1 BOTTLE (72559-021-56)Marketed from Feb 27, 2024

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)
Curist Allergy Relief
Generic name (nonproprietary)
levocetirizine dihydrochloride 5 mg
Active ingredients
Levocetirizine dihydrochloride — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Little Pharma, Inc.NDC labeler code 72559
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213513
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 72559-021_4c4b5fdc-122b-70cc-e063-6394a90a0b58SPL ID 4c4b5fdc-122b-70cc-e063-6394a90a0b58SPL set ID f2a2a5bc-2efa-c550-e053-2a95a90a55ffRxCUI 855172UNII SOD6A38AGAUPC 0372559021561
Pharmacologic class
Histamine-1 Receptor Antagonist

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

N472559002105 followed by a unit qualifier and the quantity

Package 72559-0021-05. 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)

Uses temporarily relieves these symptoms due to hay fever or other respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72559-021

What is NDC 72559-021?
72559-021 is the product NDC for Curist Allergy Relief (levocetirizine dihydrochloride 5 mg), Levocetirizine dihydrochloride 5 mg/1 tablet, listed with the FDA by Little Pharma, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Curist Allergy Relief (Levocetirizine dihydrochloride 5 mg).
What is the active ingredient?
Levocetirizine dihydrochloride.
Who is the labeler?
Little Pharma, Inc., NDC labeler code 72559. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Curist Allergy Relief?
3 other product NDCs are listed under this name. See all Curist Allergy Relief 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 Curist Allergy Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Curist Allergy Reliefloratadine 10 mgLoratadine 10 mg/1TabletOralLittle Pharma, Inc.72559-03372559-0033-4772559-0033-4872559-0033-63
Curist Allergy Relieffexofenadine hydrochloride 180 mgFexofenadine hydrochloride 180 mg/1TabletOralLittle Pharma, Inc.72559-02772559-0027-2272559-0027-2372559-0027-46
Curist Allergy Reliefcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, CoatedOralLittle Pharma, Inc.72559-00372559-0003-48

Other NDCs under ANDA 213513

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

FDA NDC Directory listings under ANDA 213513
ProductStrengthForm · routeLabelerProduct NDC
Allergy Relieflevocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralYYBA CORP73581-201
Allergy Relieflevocetirizine dihydrochloride usp, 5 mgLevocetirizine dihydrochloride 5 mg/1Tablet, CoatedOralTopco Associates, LLC76162-915
Allery Relief 24HRLevocetirizine dihydrochloride 5 mg/1Tablet, Film coatedOralAllegiant Health69168-451
Goodmeds Levocetirizine Dihydrochloride 5mg 365 countlevocetirizine dihydrochloride 5mgLevocetirizine dihydrochloride 5 mg/1TabletOralCabinet Health P.B.C.82725-4051
Levocetirizine DihydrochlorideLevocetirizine dihydrochloride 5 mg/1Tablet, Film coatedOralSportpharm LLC85766-152
Levocetirizine DihydrochlorideLevocetirizine dihydrochloride 5 mg/1Tablet, Film coatedOralFarmacias De Similares TX LLC85786-206

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