What is NDC 73581-012?

73581-012 is the product NDC for Fexofenadine, Fexofenadine hydrochloride 60 mg/1 tablet, listed with the FDA by YYBA Corp. It has 3 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?

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.

Fexofenadine NDC 73581-012 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)73581-012Labeler and product segments. Claims need a package NDC.

Product NDC at billing width73581-0012Add 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
73581-012-01	7358100120173581001201	100 TABLET in 1 BOTTLE (73581-012-01)Marketed from Sep 1, 2026
73581-012-02	7358100120273581001202	200 TABLET in 1 BOTTLE (73581-012-02)Marketed from Sep 1, 2026
73581-012-06	7358100120673581001206	60 TABLET in 1 BOTTLE (73581-012-06)Marketed from Sep 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
Generic name (nonproprietary): fexofenadine
Active ingredients: Fexofenadine hydrochloride — 60 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 219032
Marketing start: Jul 27, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 73581-012_579c7ff9-0c45-1d46-e063-6294a90aef34SPL ID 579c7ff9-0c45-1d46-e063-6294a90aef34SPL set ID 579c7ff9-0c44-1d46-e063-6294a90aef34RxCUI 997501UNII 2S068B75ZUUPC 0373581000272
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

N473581001201 followed by a unit qualifier and the quantity

Package 73581-0012-01. 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 27, 2026.

Indications (excerpt from the label)

Uses temporarily relieves these symptoms due to hay fever or other 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 73581-012

What is NDC 73581-012?: 73581-012 is the product NDC for Fexofenadine, Fexofenadine hydrochloride 60 mg/1 tablet, listed with the FDA by YYBA Corp. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Fexofenadine.
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?: 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.