NDC codes

FDA NDC Directory
Product NDC (as listed)69168-451Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69168-0451Add 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
69168-451-0669168045106120 TABLET, FILM COATED in 1 BOTTLE (69168-451-06)Marketed from Apr 2, 2024
69168-451-606916804516060 TABLET, FILM COATED in 1 BOTTLE (69168-451-60)Marketed from Apr 2, 2024
69168-451-8069168045180180 TABLET, FILM COATED in 1 BOTTLE (69168-451-80)Marketed from Mar 7, 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)
Allery Relief 24HR
Generic name (nonproprietary)
allery relief 24hr
Active ingredients
Levocetirizine dihydrochloride — 5 mg/1
Dosage form
Tablet, Film coated
Route
Oral
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 69168-451_d6893dfa-1c05-4ce7-b360-91baa94d6a69SPL ID d6893dfa-1c05-4ce7-b360-91baa94d6a69SPL set ID c523c210-b1c4-4049-9c72-2b31c9c93137RxCUI 855172UNII SOD6A38AGA
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

N469168045106 followed by a unit qualifier and the quantity

Package 69168-0451-06. 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)

Use(s) 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)

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
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
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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