What is NDC 72090-010?

72090-010 is the product NDC for Fexofenadine Hydrochloride, Fexofenadine hydrochloride 180 mg/1 tablet, listed with the FDA by Pioneer Life Sciences, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Pioneer Life Sciences, LLC, NDC labeler code 72090. 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 72090-010

NDC codes

FDA NDC Directory

Product NDC (as listed)72090-010Labeler and product segments. Claims need a package NDC.

Product NDC at billing width72090-0010Add 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
72090-010-01	7209000100172090001001	90 TABLET in 1 BOTTLE (72090-010-01)Marketed from Dec 7, 2023

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 — 180 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Pioneer Life Sciences, LLCNDC labeler code 72090
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210137
Marketing start: Dec 7, 2023
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 72090-010_2aa6e396-3103-48d1-bcd7-43b140549307SPL ID 2aa6e396-3103-48d1-bcd7-43b140549307SPL set ID d7fe71e4-aada-40f5-86a8-bf0d7eb9b851RxCUI 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

N472090001001 followed by a unit qualifier and the quantity

Package 72090-0010-01. 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 Dec 26, 2025.

Indications (excerpt from the label)

Uses 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 72090-010

What is NDC 72090-010?: 72090-010 is the product NDC for Fexofenadine Hydrochloride, Fexofenadine hydrochloride 180 mg/1 tablet, listed with the FDA by Pioneer Life Sciences, 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?: Pioneer Life Sciences, LLC, NDC labeler code 72090. 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	NUVICARE LLC	84324-045	84324-0045-01
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 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 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	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 Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	NUVICARE LLC	84324-031