What is NDC 82725-4051?

82725-4051 is the product NDC for Goodmeds Levocetirizine Dihydrochloride 5mg 365 count, Levocetirizine dihydrochloride 5 mg/1 tablet, listed with the FDA by Cabinet Health P.B.C.. It has 2 package NDCs, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Goodmeds Levocetirizine Dihydrochloride 5mg 365 count (Levocetirizine Dihydrochloride 5mg).

What is the active ingredient?

Levocetirizine dihydrochloride.

Cabinet Health P.B.C., NDC labeler code 82725. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Goodmeds Levocetirizine Dihydrochloride 5mg 365 count?

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.

NDC 82725-4051

NDC codes

FDA NDC Directory

Product NDC (as listed)82725-4051Labeler and product segments. Claims need a package NDC.

Product NDC at billing width82725-4051Add 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
82725-4051-1	8272540510182725405101	365 TABLET in 1 BOTTLE (82725-4051-1)Marketed from Jun 30, 2026
82725-4051-2	8272540510282725405102	180 TABLET in 1 BOTTLE (82725-4051-2)Marketed from Oct 5, 2026

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): Goodmeds Levocetirizine Dihydrochloride 5mg 365 count
Generic name (nonproprietary): levocetirizine dihydrochloride 5mg
Active ingredients: Levocetirizine dihydrochloride — 5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Cabinet Health P.B.C.NDC labeler code 82725
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213513
Marketing start: Jun 30, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 82725-4051_5cb46662-78a0-9d8a-e063-6294a90a8b84SPL ID 5cb46662-78a0-9d8a-e063-6294a90a8b84
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

N482725405101 followed by a unit qualifier and the quantity

Package 82725-4051-01. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 82725-4051

What is NDC 82725-4051?: 82725-4051 is the product NDC for Goodmeds Levocetirizine Dihydrochloride 5mg 365 count, Levocetirizine dihydrochloride 5 mg/1 tablet, listed with the FDA by Cabinet Health P.B.C.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Goodmeds Levocetirizine Dihydrochloride 5mg 365 count (Levocetirizine Dihydrochloride 5mg).
What is the active ingredient?: Levocetirizine dihydrochloride.
Who is the labeler?: Cabinet Health P.B.C., NDC labeler code 82725. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Goodmeds Levocetirizine Dihydrochloride 5mg 365 count?: 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 213513

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

FDA NDC Directory listings under ANDA 213513
Product	Strength	Form · route	Labeler	Product NDC
Allergy Relieflevocetirizine dihydrochloride	Levocetirizine dihydrochloride 5 mg/1	TabletOral	YYBA CORP	73581-201
Allergy Relieflevocetirizine dihydrochloride usp, 5 mg	Levocetirizine dihydrochloride 5 mg/1	Tablet, CoatedOral	Topco Associates, LLC	76162-915
Allery Relief 24HR	Levocetirizine dihydrochloride 5 mg/1	Tablet, Film coatedOral	Allegiant Health	69168-451
Curist Allergy Relieflevocetirizine dihydrochloride 5 mg	Levocetirizine dihydrochloride 5 mg/1	TabletOral	Little Pharma, Inc.	72559-021
Levocetirizine Dihydrochloride	Levocetirizine dihydrochloride 5 mg/1	Tablet, Film coatedOral	Sportpharm LLC	85766-152
Levocetirizine Dihydrochloride	Levocetirizine dihydrochloride 5 mg/1	Tablet, Film coatedOral	Farmacias De Similares TX LLC	85786-206

Goodmeds Levocetirizine Dihydrochloride 5mg 365 count (Levocetirizine dihydrochloride 5mg) NDC 82725-4051