NDC codes

FDA NDC Directory
Product NDC (as listed)73581-201Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73581-0201Add 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
73581-201-18735810201181 BOTTLE in 1 BOX (73581-201-18) / 18 TABLET in 1 BOTTLEMarketed from Dec 2, 2025
73581-201-36735810201362 BOTTLE in 1 CARTON (73581-201-36) / 180 TABLET in 1 BOTTLEMarketed from Jun 30, 2020
73581-201-80735810201801 BOTTLE in 1 BOX (73581-201-80) / 180 TABLET in 1 BOTTLEMarketed from Jun 30, 2020

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)
Allergy Relief
Generic name (nonproprietary)
levocetirizine dihydrochloride
Active ingredients
Levocetirizine dihydrochloride — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
YYBA CORP
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 73581-201_5bc38f40-5a86-6dba-e063-6394a90ab9bdSPL ID 5bc38f40-5a86-6dba-e063-6394a90ab9bd
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

N473581020118 followed by a unit qualifier and the quantity

Package 73581-0201-18. 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

The FDA listing for this product does not reference a label (SPL) set.

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
Goodmeds Levocetirizine Dihydrochloride 5mg 365 countlevocetirizine dihydrochloride 5mgLevocetirizine dihydrochloride 5 mg/1TabletOralCabinet Health P.B.C.82725-4051
Curist Allergy Relieflevocetirizine dihydrochloride 5 mgLevocetirizine dihydrochloride 5 mg/1TabletOralLittle Pharma, Inc.72559-021
Curist Allergy Relieflevocetirizine dihydrochloride 5 mgLevocetirizine dihydrochloride 5 mg/1TabletOralLittle Pharma, Inc.72559-021
Allery Relief 24HRLevocetirizine dihydrochloride 5 mg/1Tablet, Film coatedOralAllegiant Health69168-451
Levocetirizine DihydrochlorideLevocetirizine dihydrochloride 5 mg/1Tablet, Film coatedOralFarmacias De Similares TX LLC85786-206
Levocetirizine DihydrochlorideLevocetirizine dihydrochloride 5 mg/1Tablet, Film coatedOralSportpharm LLC85766-152
Levocetirizine DihydrochlorideLevocetirizine dihydrochloride 5 mg/1Tablet, Film coatedOralCamber Consumer Care Inc69230-321

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