What is NDC 10267-3579?

10267-3579 is the product NDC for Cetirizine Hydrochloride 10 mg, Cetirizine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Contract Pharmacal Corp.. It has 5 package NDCs, shown above in 10- and 11-digit form.

Contract Pharmacal Corp., NDC labeler code 10267. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Cetirizine Hydrochloride 10 mg?

3 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Cetirizine Hydrochloride 10 mg NDC 10267-3579

NDC codes

FDA NDC Directory

Product NDC (as listed)10267-3579Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10267-3579Add 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 NDC	11-digit (billing)	Package
10267-3579-1	1026735790110267357901	1 BOTTLE in 1 CARTON (10267-3579-1) / 100 TABLET, FILM COATED in 1 BOTTLEMarketed from Dec 31, 2025
10267-3579-3	1026735790310267357903	1 BOTTLE in 1 CARTON (10267-3579-3) / 30 TABLET, FILM COATED in 1 BOTTLEMarketed from Dec 31, 2025
10267-3579-4	1026735790410267357904	100 TABLET, FILM COATED in 1 BOTTLE (10267-3579-4)Marketed from May 31, 2025
10267-3579-6	1026735790610267357906	365 TABLET, FILM COATED in 1 BOTTLE (10267-3579-6)Marketed from Apr 16, 2025
10267-3579-7	1026735790710267357907	1 BOTTLE in 1 CARTON (10267-3579-7) / 60 TABLET, FILM COATED in 1 BOTTLEMarketed from Dec 31, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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): Cetirizine Hydrochloride 10 mg
Generic name (nonproprietary): cetirizine hydrochloride 10 mg
Active ingredients: Cetirizine hydrochloride — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Contract Pharmacal Corp.NDC labeler code 10267
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076047
Marketing start: Apr 16, 2025
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 10267-3579_3633ac85-4814-e6a7-e063-6294a90a375dSPL ID 3633ac85-4814-e6a7-e063-6294a90a375dSPL set ID 84459f11-3405-4a8e-be38-333b7de2a578RxCUI 1014678UNII 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

N410267357901 followed by a unit qualifier and the quantity

Package 10267-3579-01. 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 May 28, 2025.

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)

About NDC 10267-3579

What is NDC 10267-3579?: 10267-3579 is the product NDC for Cetirizine Hydrochloride 10 mg, Cetirizine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Contract Pharmacal Corp.. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Cetirizine Hydrochloride 10 mg.
What is the active ingredient?: Cetirizine hydrochloride.
Who is the labeler?: Contract Pharmacal Corp., NDC labeler code 10267. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cetirizine Hydrochloride 10 mg?: 3 other product NDCs are listed under this name. See all Cetirizine Hydrochloride 10 mg 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 Cetirizine Hydrochloride 10 mg NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Cetirizine Hydrochloride 10 Mgcetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	TWIN MED, LLC	55681-302	55681-0302-03
Cetirizine Hydrochloride 10 Mgcetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	YYBA CORP	73581-202	73581-0202-0173581-0202-05
Cetirizine Hydrochloride 10 Mgcetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	SDA Laboratories, Inc.	66424-564	66424-0564-0166424-0564-05

Other NDCs under ANDA 076047

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

FDA NDC Directory listings under ANDA 076047
Product	Strength	Form · route	Labeler	Product NDC
Cetirizine HClcetirizine	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	GERI-CARE PHARMACEUTICAL CORP	57896-992
cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	72789-458
Cetirizine Hydrochloride	Cetirizine hydrochloride 5 mg/1	TabletOral	First Nation Group, LLC	81469-352
Cetirizine Hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	First Nation Group, LLC	81469-353
Dr Simi Cetirizine Hydrochloride 10 mgcetirizine hydrochloride 10 mg	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Farmacias De Similares TX LLC	85786-203