What is NDC 0113-0241?

0113-0241 is the product NDC for good sense levocetirizine (levocetirizine dihydrochloride), Levocetirizine dihydrochloride 5 mg/1 tablet, film coated, listed with the FDA by L. Perrigo Company. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

good sense levocetirizine (Levocetirizine dihydrochloride).

What is the active ingredient?

Levocetirizine dihydrochloride.

L. Perrigo Company, NDC labeler code 0113. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for good sense levocetirizine?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

good sense levocetirizine NDC 0113-0241

NDC codes

FDA NDC Directory

Product NDC (as listed)0113-0241Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00113-0241Add 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
0113-0241-01	0011302410100113024101	1 BOTTLE in 1 CARTON (0113-0241-01) / 35 TABLET, FILM COATED in 1 BOTTLEMarketed from Sep 11, 2020
0113-0241-27	0011302412700113024127	1 BOTTLE in 1 CARTON (0113-0241-27) / 80 TABLET, FILM COATED in 1 BOTTLE (0113-0241-00)Marketed from Jun 18, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): good sense levocetirizine
Generic name (nonproprietary): levocetirizine dihydrochloride
Active ingredients: Levocetirizine dihydrochloride — 5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: L. Perrigo CompanyNDC labeler code 0113
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211983
Marketing start: Sep 11, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 0113-0241_cda5617c-c2ca-4c27-8af9-2c1743c043ebSPL ID cda5617c-c2ca-4c27-8af9-2c1743c043ebSPL set ID 0b482364-a00a-4b95-975a-f403a3ae4d2eRxCUI 855172UNII SOD6A38AGAUPC 0301130241012
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

N400113024101 followed by a unit qualifier and the quantity

Package 00113-0241-01. 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 Jul 13, 2026.

Indications (excerpt from the label)

Uses temporarily relieves these symptoms due to hay fever or other respiratory allergies: • runny nose • itchy, watery eyes • sneezing • 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 0113-0241

What is NDC 0113-0241?: 0113-0241 is the product NDC for good sense levocetirizine (levocetirizine dihydrochloride), Levocetirizine dihydrochloride 5 mg/1 tablet, film coated, listed with the FDA by L. Perrigo Company. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: good sense levocetirizine (Levocetirizine dihydrochloride).
What is the active ingredient?: Levocetirizine dihydrochloride.
Who is the labeler?: L. Perrigo Company, NDC labeler code 0113. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for good sense levocetirizine?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 211983

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

FDA NDC Directory listings under ANDA 211983
Product	Strength	Form · route	Labeler	Product NDC
allergy relieflevocetirizine dihydrochloride	Levocetirizine dihydrochloride 5 mg/1	Tablet, Film coatedOral	Walgreen Company	0363-3901
allergy relieflevocetirizine dihydrochloride	Levocetirizine dihydrochloride 5 mg/1	Tablet, Film coatedOral	Rite Aid Corporation	11822-0241
Allergy Relieflevocetirizine dihydrochloride	Levocetirizine dihydrochloride 5 mg/1	Tablet, Film coatedOral	Meijer Distribution Inc	41250-488
Allergy Relieflevocetirizine dihydrochloride	Levocetirizine dihydrochloride 5 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-784
basic care allergy relieflevocetirizine dihydrochloride	Levocetirizine dihydrochloride 5 mg/1	Tablet, Film coatedOral	Amazon.com Services LLC	72288-241
DG Health Allergy Relieflevocetirizine dihydrochloride	Levocetirizine dihydrochloride 5 mg/1	Tablet, Film coatedOral	Dolgencorp, LLC	55910-241
Topcare All Day Allergylevocetirizine dihydrochloride	Levocetirizine dihydrochloride 5 mg/1	Tablet, Film coatedOral	Topco Associates LLC	36800-241

good sense levocetirizine (Levocetirizine dihydrochloride) NDC 0113-0241