What is NDC 53943-519?

53943-519 is the product NDC for Cetirizine Hydrochloride, Cetirizine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Discount Drug Mart, Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.

Discount Drug Mart, Inc, NDC labeler code 53943. 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?

107 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 NDC 53943-519

NDC codes

FDA NDC Directory

Product NDC (as listed)53943-519Labeler and product segments. Claims need a package NDC.

Product NDC at billing width53943-0519Add 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	Copy
53943-519-30	5394305193053943051930	1 BOTTLE in 1 CARTON (53943-519-30) / 30 TABLET, FILM COATED in 1 BOTTLEMarketed from Jan 20, 2020
53943-519-45	5394305194553943051945	1 BOTTLE in 1 CARTON (53943-519-45) / 45 TABLET, FILM COATED in 1 BOTTLEMarketed from Jan 20, 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): Cetirizine Hydrochloride
Generic name (nonproprietary): cetirizine hydrochloride
Active ingredients: Cetirizine hydrochloride — 10 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Discount Drug Mart, IncNDC labeler code 53943
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078343
Marketing start: Jan 20, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 53943-519_5c71a4a6-cf88-4fdc-db4f-23235af0306bSPL ID 5c71a4a6-cf88-4fdc-db4f-23235af0306bSPL set ID c7c7e496-3682-c764-88ef-d2a09823f71eRxCUI 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

N453943051930 followed by a unit qualifier and the quantity

Package 53943-0519-30. 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 Jul 16, 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 53943-519

What is NDC 53943-519?: 53943-519 is the product NDC for Cetirizine Hydrochloride, Cetirizine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Discount Drug Mart, Inc. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Cetirizine Hydrochloride.
What is the active ingredient?: Cetirizine hydrochloride.
Who is the labeler?: Discount Drug Mart, Inc, NDC labeler code 53943. 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?: 107 other product NDCs are listed under this name. See all Cetirizine Hydrochloride 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 NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Cetirizine Hydrochloride	Cetirizine hydrochloride 5 mg/1	TabletOral	First Nation Group, LLC	81469-352	81469-0352-01
Cetirizine Hydrochloride	Cetirizine hydrochloride 10 mg/1	TabletOral	First Nation Group, LLC	81469-353	81469-0353-0181469-0353-0381469-0353-05+1 more
Cetirizine Hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Safecor Health, LLC	48433-017	48433-0017-20
Cetirizine hydrochloride	Cetirizine hydrochloride 1 mg/mL	SolutionOral	Advagen Pharma Ltd.,	72888-480	72888-0480-01
cetirizine hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-4072	68788-4072-0368788-4072-0668788-4072-09
Cetirizine Hydrochloride	Cetirizine hydrochloride 1 mg/mL	SolutionOral	Bionpharma Inc.	69452-426	69452-0426-5569452-0426-88
Cetirizine Hydrochloride	Cetirizine hydrochloride 1 mg/mL	SolutionOral	Rising Pharma Holdings, Inc.	57237-357	57237-0357-1257237-0357-24
Cetirizine Hydrochloride	Cetirizine hydrochloride 1 mg/mL	SolutionOral	Rising Pharma Holdings, Inc.	57237-358	57237-0358-1257237-0358-24
Cetirizine Hydrochloride	Cetirizine hydrochloride 1 mg/mL	SolutionOral	BAJAJ MEDICAL, LLC	61037-480	61037-0480-2261037-0480-2361037-0480-24+2 more
Cetirizine Hydrochloride	Cetirizine hydrochloride 1 mg/mL	SolutionOral	BAJAJ MEDICAL, LLC	61037-480	61037-0480-0261037-0480-0361037-0480-04+2 more

All 108 Cetirizine Hydrochloride NDCs

Other NDCs under ANDA 078343

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

FDA NDC Directory listings under ANDA 078343
Product	Strength	Form · route	Labeler	Product NDC
Cetirizine Hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Dr.Reddy's Laboratories Limited	55111-699
Cetirizine Hydrochloridecetirizine hydrochloride tablets	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	VERITYRX, LLC	83939-0004
cetirizine hydrochloridecetirizine hydrochloride tablets	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Strategic Sourcing Services LLC	70677-1007
Cetirizine Hydrochloridecetirizine hydrochloride tablets	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Sportpharm LLC	85766-045
Cetirizine Hydrochloride	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Dr.Reddy's Laboratories Limited	55111-351
Cetirizine Hydrochloridecetirizine hydrochloride tablets	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Dr. Reddy's Laboratories Inc.	43598-183
Cetirizine Hydrochloridecetirizine hydrochloride tablets	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Dr. Reddy's Laboratories Inc.	43598-811
Cetirizine Hydrochloridecetirizine hydrochloride tablets	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Proficient Rx LP	71205-709
Cetirizine Hydrochloridecetirizine hydrochloride tablets	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-9612
Cetirizine Hydrochloridecetirizine hydrochloride tablets	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-801
Cetirizine Hydrochloridecetirizine hydrochloride tablets	Cetirizine hydrochloride 10 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8435