NDC codes

FDA NDC Directory
Product NDC (as listed)67751-192Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67751-0192Add 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
67751-192-01677510192011 POUCH in 1 CARTON (67751-192-01) / 1 TABLET, FILM COATED in 1 POUCHMarketed from Nov 20, 2019

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)
Zyrtec Allergy
Generic name (nonproprietary)
cetirizine hydrochloride
Active ingredients
Cetirizine hydrochloride — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Over-the-counter drug
Marketing category
NDA — New Drug ApplicationApplication NDA 019835
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 67751-192_f70c23f1-f2a8-8415-e053-6394a90a64dcSPL ID f70c23f1-f2a8-8415-e053-6394a90a64dcSPL set ID 9c4693cb-f066-0666-e053-2a95a90a96d3RxCUI 1014678, 1020026UNII 64O047KTOA
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

N467751019201 followed by a unit qualifier and the quantity

Package 67751-0192-01. 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 upper 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 NDA 019835

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

FDA NDC Directory listings under NDA 019835
ProductStrengthForm · routeLabelerProduct NDC
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralMorning Star OTC53209-5001
ZYRTEC Hivescetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralKenvue Brands LLC50580-116
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralSelect Consumer Group85237-2960
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralKenvue Brands LLC50580-726
Zyrtec Allergycetirizine hydrochloride—KitKenvue Brands LLC50580-752
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 5 mg/1Tablet, Film coatedOralKenvue Brands LLC50580-754
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralSavings Distributors LLC73097-016
Zyrtec Allergycetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralRedPharm Drug Inc67296-1484
Zyrtec Allergy, Lil Drug Storecetirizine hydrochloride tablet, film coatedCetirizine hydrochloride 10 mg/1Tablet, Film coatedOralLil' Drug Store Products, Inc.66715-9811

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