What is NDC 84324-045?

84324-045 is the product NDC for Fexofenadine Hydrochloride, Fexofenadine hydrochloride 60 mg/1 tablet, listed with the FDA by NUVICARE LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

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 Fexofenadine Hydrochloride?

42 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Fexofenadine Hydrochloride NDC 84324-045

NDC codes

FDA NDC Directory

Product NDC (as listed)84324-045Labeler and product segments. Claims need a package NDC.

Product NDC at billing width84324-0045Add 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
84324-045-01	8432400450184324004501	60 TABLET in 1 BOTTLE (84324-045-01)Marketed from Jul 30, 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): Fexofenadine Hydrochloride
Generic name (nonproprietary): fexofenadine hydrochloride
Active ingredients: Fexofenadine hydrochloride — 60 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 204507
Marketing start: Jul 30, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 84324-045_fdf1d6d1-054f-42e6-b4fc-b72f70bbe235SPL ID fdf1d6d1-054f-42e6-b4fc-b72f70bbe235SPL set ID dd0da52b-fc82-4ec9-854c-0d7c52e926fbRxCUI 997501UNII 2S068B75ZUUPC 0384324000602
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

N484324004501 followed by a unit qualifier and the quantity

Package 84324-0045-01. 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 Aug 3, 2026.

Indications (excerpt from the label)

Uses ■ temporarily relieves these symptoms due to hay fever or other upper 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 84324-045

What is NDC 84324-045?: 84324-045 is the product NDC for Fexofenadine Hydrochloride, Fexofenadine hydrochloride 60 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?: 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 Fexofenadine Hydrochloride?: 42 other product NDCs are listed under this name. See all Fexofenadine 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 Fexofenadine Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Fexofenadine Hydrochloridefexofenadine hydrochloride oral	Fexofenadine hydrochloride 30 mg/5mL	SuspensionOral	Aurohealth LLC	58602-427	58602-0427-2058602-0427-24
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 60 mg/1	TabletOral	YYBA Corp	73581-025	73581-0025-0173581-0025-0673581-0025-20
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	YYBA Corp	73581-026	73581-0026-0173581-0026-1073581-0026-20
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	YYBA Corp	73581-027	73581-0027-0173581-0027-0473581-0027-10+1 more
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	AMZ789 LLC	73629-008	73629-0008-03
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	NUVICARE LLC	84324-008	84324-0008-01
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	AMERISOURCE BERGEN	46122-779	46122-0779-5846122-0779-6146122-0779-66
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Pioneer Life Sciences, LLC	72090-010	72090-0010-01
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 60 mg/1	Tablet, Film coatedOral	Granules India Limited	62207-889	62207-0889-4962207-0889-5162207-0889-60
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Granules India Limited	62207-891	62207-0891-4962207-0891-5162207-0891-58

All 43 Fexofenadine Hydrochloride NDCs

Other NDCs under ANDA 204507

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

FDA NDC Directory listings under ANDA 204507
Product	Strength	Form · route	Labeler	Product NDC
IAllergy Relieffexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, CoatedOral	Safeway, Inc.	21130-405
fexofenadine hcl	Fexofenadine hydrochloride 60 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2165
Allergy Relieffexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, CoatedOral	P & L Development, LLC	59726-701
fexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-893
Curist Allergy Relieffexofenadine hydrochloride 180 mg	Fexofenadine hydrochloride 180 mg/1	TabletOral	Little Pharma, Inc.	72559-027
Allergy Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Magno-Humphries, Inc.	54257-170
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Akron Pharma Inc.	71399-8042
Curist Hives Relieffexofenadine hydrochloride 180 mg	Fexofenadine hydrochloride 180 mg/1	TabletOral	Little Pharma, Inc.	72559-028
Allergy Relieffexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, CoatedOral	P & L Development, LLC	59726-801
fexofenadine hcl	Fexofenadine hydrochloride 60 mg/1	Tablet, Film coatedOral	AKRON PHARMA INC	71399-8659
fexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-905
Fexofenadine HCl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-921
Allergy Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	YYBA CORP	73581-011
Allergy Relieffexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Bi-Mart	37835-601
Fexofenadine HCl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Camber Consumer Care	69230-202
Fexofenadine HCl	Fexofenadine hydrochloride 60 mg/1	Tablet, Film coatedOral	Camber Consumer Care	69230-201
Allergy Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 60 mg/1	TabletOral	YYBA CORP	73581-103
fexofenadine hcl	Fexofenadine hydrochloride 60 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7192
fexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Radha Pharmaceuticals	77771-202
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	SPIRIT PHARMACEUTICALS LLC	68210-2210

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