What is NDC 68210-2210?

68210-2210 is the product NDC for Fexofenadine Hydrochloride, Fexofenadine hydrochloride 180 mg/1 tablet, film coated, listed with the FDA by SPIRIT PHARMACEUTICALS LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

SPIRIT PHARMACEUTICALS LLC, NDC labeler code 68210. 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 68210-2210

NDC codes

FDA NDC Directory

Product NDC (as listed)68210-2210Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68210-2210Add 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
68210-2210-1	6821022100168210221001	100 TABLET, FILM COATED in 1 PACKAGE (68210-2210-1)Marketed from Mar 17, 2020

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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: SPIRIT PHARMACEUTICALS LLCNDC labeler code 68210
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204507
Marketing start: Mar 17, 2020
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 68210-2210_292e71ee-f44d-0821-e063-6394a90a4187SPL ID 292e71ee-f44d-0821-e063-6394a90a4187SPL set ID ae0f16f6-d07a-47e1-adb8-07803c6cfb13RxCUI 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

N468210221001 followed by a unit qualifier and the quantity

Package 68210-2210-01. 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 13, 2024.

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 68210-2210

What is NDC 68210-2210?: 68210-2210 is the product NDC for Fexofenadine Hydrochloride, Fexofenadine hydrochloride 180 mg/1 tablet, film coated, listed with the FDA by SPIRIT PHARMACEUTICALS 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?: SPIRIT PHARMACEUTICALS LLC, NDC labeler code 68210. 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 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 Hydrochloride	Fexofenadine hydrochloride 60 mg/1	TabletOral	NUVICARE LLC	84324-045
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

Showing 20 of 29.