What is NDC 84324-031?

84324-031 is the product NDC for Nuvicare Hives Relief (fexofenadine hydrochloride), Fexofenadine hydrochloride 180 mg/1 tablet, listed with the FDA by NUVICARE LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Nuvicare Hives Relief (Fexofenadine hydrochloride).

NUVICARE LLC, NDC labeler code 84324. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Nuvicare Hives Relief?

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.

Nuvicare Hives Relief NDC 84324-031

NDC codes

FDA NDC Directory

Product NDC (as listed)84324-031Labeler and product segments. Claims need a package NDC.

Product NDC at billing width84324-0031Add 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
84324-031-01	8432400310184324003101	30 TABLET in 1 BOTTLE (84324-031-01)Marketed from Jan 21, 2026

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): Nuvicare Hives Relief
Generic name (nonproprietary): fexofenadine hydrochloride
Active ingredients: Fexofenadine hydrochloride — 180 mg/1
Dosage form: Tablet
Route: Oral
Labeler: NUVICARE LLCNDC labeler code 84324
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210137
Marketing start: Jan 21, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 84324-031_8a758eab-e855-4cac-85e1-c7df0aa2150dSPL ID 8a758eab-e855-4cac-85e1-c7df0aa2150dSPL set ID a8e11094-ca69-488d-a720-b8129f17f505RxCUI 997420UNII 2S068B75ZU
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

N484324003101 followed by a unit qualifier and the quantity

Package 84324-0031-01. 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 Jan 21, 2026.

Indications (excerpt from the label)

Uses reduces hives and relieves itching due to hives (urticaria). This product will not prevent hives or an allergic skin reaction from occurring.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 84324-031

What is NDC 84324-031?: 84324-031 is the product NDC for Nuvicare Hives Relief (fexofenadine hydrochloride), Fexofenadine hydrochloride 180 mg/1 tablet, listed with the FDA by NUVICARE LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Nuvicare Hives Relief (Fexofenadine hydrochloride).
What is the active ingredient?: Fexofenadine hydrochloride.
Who is the labeler?: NUVICARE LLC, NDC labeler code 84324. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nuvicare Hives Relief?: 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 210137

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

FDA NDC Directory listings under ANDA 210137
Product	Strength	Form · route	Labeler	Product NDC
CVS Fexofenadine Hydrochloridefexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	CVS Pharmacy	51316-183
FEXOFENADINE HCl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Strategic Sourcing Services, LLC	70677-1239
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Pioneer Life Sciences, LLC	72090-010
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	YYBA Corp	73581-027
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	NUVICARE LLC	84324-008
Gencare Hives Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Pioneer Life Sciences, LLC	72090-058

Nuvicare Hives Relief (Fexofenadine hydrochloride) NDC 84324-031