What is NDC 71399-8042?

71399-8042 is the product NDC for Fexofenadine HCL, Fexofenadine hydrochloride 180 mg/1 tablet, listed with the FDA by Akron Pharma Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Akron Pharma Inc., NDC labeler code 71399. 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 71399-8042 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71399-8042Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71399-8042Add 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
71399-8042-1	7139980420171399804201	100 TABLET in 1 BOTTLE (71399-8042-1)Marketed from Sep 9, 2020
71399-8042-3	7139980420371399804203	30 TABLET in 1 BOTTLE (71399-8042-3)Marketed from Aug 9, 2024

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 HCL
Generic name (nonproprietary): fexofenadine hcl
Active ingredients: Fexofenadine hydrochloride — 180 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Akron Pharma Inc.NDC labeler code 71399
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204507
Marketing start: Sep 9, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 71399-8042_8ac3ac9a-206b-446a-87c9-bda3b8441cd4SPL ID 8ac3ac9a-206b-446a-87c9-bda3b8441cd4SPL set ID 08023b99-0634-4ac9-afd6-4f2d2e0d2c8aRxCUI 997420UNII 2S068B75ZUUPC 0377399204235, 0371399804211
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

N471399804201 followed by a unit qualifier and the quantity

Package 71399-8042-01. 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 Aug 20, 2024.

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 71399-8042

What is NDC 71399-8042?: 71399-8042 is the product NDC for Fexofenadine HCL, Fexofenadine hydrochloride 180 mg/1 tablet, listed with the FDA by Akron Pharma Inc.. It has 2 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?: Akron Pharma Inc., NDC labeler code 71399. 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 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
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
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	Tablet, Film coatedOral	SPIRIT PHARMACEUTICALS LLC	68210-2210

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