What is NDC 73581-009?

73581-009 is the product NDC for Fexofenadine HCL, Fexofenadine hydrochloride 180 mg/1 tablet, listed with the FDA by YYBA Corp. It has 4 package NDCs, shown above in 10- and 11-digit form.

YYBA Corp, NDC labeler code 73581. 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 HCL?

45 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Fexofenadine HCL NDC 73581-009 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)73581-009Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73581-0009Add 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
73581-009-01	7358100090173581000901	10 TABLET in 1 BOTTLE (73581-009-01)Marketed from Jan 1, 2026
73581-009-04	7358100090473581000904	40 TABLET in 1 BOTTLE (73581-009-04)Marketed from Jan 1, 2026
73581-009-10	7358100091073581000910	100 TABLET in 1 BOTTLE (73581-009-10)Marketed from Jan 1, 2026
73581-009-20	7358100092073581000920	200 TABLET in 1 BOTTLE (73581-009-20)Marketed from Jan 1, 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 HCL
Generic name (nonproprietary): fexofenadine hcl
Active ingredients: Fexofenadine hydrochloride — 180 mg/1
Dosage form: Tablet
Route: Oral
Labeler: YYBA CorpNDC labeler code 73581
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204097
Marketing start: Aug 19, 2016
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 73581-009_52d50de4-dca4-33ff-e063-6394a90a1b09SPL ID 52d50de4-dca4-33ff-e063-6394a90a1b09SPL set ID 52d50976-e63a-b3e3-e063-6294a90a6a97RxCUI 997420, 997501UNII 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

N473581000901 followed by a unit qualifier and the quantity

Package 73581-0009-01. 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 1, 2026.

Indications (excerpt from the label)

USE(S) 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 73581-009

What is NDC 73581-009?: 73581-009 is the product NDC for Fexofenadine HCL, Fexofenadine hydrochloride 180 mg/1 tablet, listed with the FDA by YYBA Corp. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Fexofenadine HCL.
What is the active ingredient?: Fexofenadine hydrochloride.
Who is the labeler?: YYBA Corp, NDC labeler code 73581. 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 HCL?: 45 other product NDCs are listed under this name. See all Fexofenadine HCL 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 HCL NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Fexofenadine HCL	Fexofenadine hydrochloride 60 mg/1	TabletOral	YYBA Corp	73581-010	73581-0010-0173581-0010-0673581-0010-10+1 more
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Walmart Inc.	79903-358	79903-0358-3079903-0358-4579903-0358-90
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Strategic Sourcing Services	70677-1256	70677-1256-0170677-1256-02
fexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Aphena Pharma Solutions - Tennessee, LLC	71610-905	71610-0905-3071610-0905-5371610-0905-60+1 more
fexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Radha Pharmaceuticals	77771-202	77771-0202-0177771-0202-0577771-0202-30
fexofenadine hcl	Fexofenadine hydrochloride 60 mg/1	Tablet, Film coatedOral	Radha Pharmaceuticals	77771-201	77771-0201-0177771-0201-05
Fexofenadine HCl	Fexofenadine hydrochloride 180 mg/1	TabletOral	Rite Aid	11822-7661	11822-7661-05
Fexofenadine HCl	Fexofenadine hydrochloride 60 mg/1	TabletOral	Rite Aid	11822-7652	11822-7652-04
Fexofenadine HCl	Fexofenadine hydrochloride 180 mg/1	TabletOral	Rite Aid	11822-7663	11822-7663-04
Fexofenadine HCl	Fexofenadine hydrochloride 180 mg/1	TabletOral	Rite Aid	11822-7660	11822-7660-0311822-7660-0711822-7660-09

All 46 Fexofenadine HCL NDCs

Other NDCs under ANDA 204097

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

FDA NDC Directory listings under ANDA 204097
Product	Strength	Form · route	Labeler	Product NDC
24HR Allergy Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	CARDINAL HEALTH 110, LLC. DBA LEADER	70000-0726
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	A-S Medication Solutions	50090-6965
equate allergy relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Walmart Inc.	49035-366
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	A-S Medication Solutions	50090-4070
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Walmart Inc.	79903-358
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Camber Consumer Care	69230-300
Fexofenadine HCL	Fexofenadine hydrochloride 60 mg/1	TabletOral	Camber Consumer Care	69230-301
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	A-S Medication Solutions	50090-4267
Allergy Relieffexofenadine hcl	Fexofenadine hydrochloride 60 mg/1	Tablet, CoatedOral	PLD Acquisitions LLC DBA Avma Pharma Solutions	63548-0663
Childrens Allergy Relieffexofenadine hcl	Fexofenadine hydrochloride 30 mg/1	TabletOral	PLD Acquisitions LLC DBA Avma Pharma Solutions	63548-0662
Allergy Relieffexofenadine hcl	Fexofenadine hydrochloride 180 mg/1	TabletOral	PLD Acquisitions LLC DBA Avma Pharma Solutions	63548-0664
Equatefexofenadine hydrochloride tablets	Fexofenadine hydrochloride 180 mg/1	TabletOral	Walmart Inc	79903-441
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Northwind Health Company, LLC	51655-854
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Bryant Ranch Prepack	71335-1217
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Proficient Rx LP	71205-531
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	NorthStar RxLLC	16714-899
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Strategic Sourcing Services	70677-1256
Fexofenadine HCL	Fexofenadine hydrochloride 60 mg/1	TabletOral	YYBA Corp	73581-010
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	72789-196
Fexofenadine HCL	Fexofenadine hydrochloride 180 mg/1	TabletOral	Preferred Pharmaceuticals, Inc.	68788-7449

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