What is NDC 10202-229?

10202-229 is the product NDC for Fexofenadine hydrochloride, Fexofenadine hydrochloride 180 mg/1 tablet, film coated, listed with the FDA by 7-eleven. It has 1 package NDC, shown above in 10- and 11-digit form.

7-eleven, NDC labeler code 10202. 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 10202-229

NDC codes

FDA NDC Directory

Product NDC (as listed)10202-229Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10202-0229Add 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
10202-229-66	1020202296610202022966	1 BLISTER PACK in 1 CARTON (10202-229-66) / 10 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Jan 15, 2015

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, Film coated
Route: Oral
Labeler: 7-elevenNDC labeler code 10202
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202039
Marketing start: Jan 15, 2015
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 10202-229_d5914c05-e8db-4c79-82d0-a279d1304118SPL ID d5914c05-e8db-4c79-82d0-a279d1304118SPL set ID d5914c05-e8db-4c79-82d0-a279d1304118RxCUI 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

N410202022966 followed by a unit qualifier and the quantity

Package 10202-0229-66. 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 Jun 20, 2019.

Indications (excerpt from the label)

Uses temporarily relieves these symptoms due to hay fever or other upper resporatory 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 10202-229

What is NDC 10202-229?: 10202-229 is the product NDC for Fexofenadine hydrochloride, Fexofenadine hydrochloride 180 mg/1 tablet, film coated, listed with the FDA by 7-eleven. 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?: 7-eleven, NDC labeler code 10202. 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 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

All 43 Fexofenadine hydrochloride NDCs

Other NDCs under ANDA 202039

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

FDA NDC Directory listings under ANDA 202039
Product	Strength	Form · route	Labeler	Product NDC
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 30 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-876
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 60 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-877
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	Aurohealth LLC	58602-878