NDC codes

FDA NDC Directory
Product NDC (as listed)69842-961Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69842-0961Add 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
69842-961-76698420961764 BLISTER PACK in 1 CARTON (69842-961-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Feb 1, 2021

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)
Childrens Cetirizine Hydrochloride
Generic name (nonproprietary)
cetirizine hydrochloride
Active ingredients
Cetirizine hydrochloride — 10 mg/1
Dosage form
Tablet, Orally disintegrating
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213557
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 69842-961_c4c715b2-8239-4b57-bfd9-c3c4ddea19c1SPL ID c4c715b2-8239-4b57-bfd9-c3c4ddea19c1SPL set ID b955c7ed-29da-959f-e053-2a95a90a03d4RxCUI 1011482UNII 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

N469842096176 followed by a unit qualifier and the quantity

Package 69842-0961-76. 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 ANDA 213557

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

FDA NDC Directory listings under ANDA 213557
ProductStrengthForm · routeLabelerProduct NDC
Childrens Cetirizine Hydrochloridecetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralAurohealth LLC58602-856
Cetirizine HydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralAurohealth LLC58602-860
Cetirizine HydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralAurohealth LLC58602-862
Cetirizine HydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralWALGREEN CO.0363-0471
Cetirizine HydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralCVS Pharmacy, Inc.69842-234
Cetirizine HydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralTOPCO ASSOCIATES LLC76162-009
Childrens Cetirizine Hydrochloridecetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralWALGREEN CO.0363-4025
Cetirizine HydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralKROGER COMPANY30142-058
Childrens Cetirizine Hydrochloridecetirizine hydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralWALMART INC.79903-406
Cetirizine HydrochlorideCetirizine hydrochloride 10 mg/1Tablet, Orally disintegratingOralAurohealth LLC58602-838

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