What is NDC 43598-936?

43598-936 is the product NDC for Fexofenadine Hydrochloride, Fexofenadine hydrochloride 60 mg/1 tablet, listed with the FDA by Dr. Reddy's Laboratories Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Dr. Reddy's Laboratories Inc., NDC labeler code 43598. 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 43598-936

NDC codes

FDA NDC Directory

Product NDC (as listed)43598-936Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43598-0936Add 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
43598-936-01	4359809360143598093601	1 BOTTLE in 1 CARTON (43598-936-01) / 100 TABLET in 1 BOTTLEMarketed from Dec 1, 2020

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 — 60 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Dr. Reddy's Laboratories Inc.NDC labeler code 43598
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076502
Marketing start: Dec 1, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 43598-936_ee1ae5bd-d3dc-23a2-c1f3-c25b2ec57b1cSPL ID ee1ae5bd-d3dc-23a2-c1f3-c25b2ec57b1cSPL set ID b0121213-eae1-8429-9986-3b3b26f35e47RxCUI 997501UNII 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

N443598093601 followed by a unit qualifier and the quantity

Package 43598-0936-01. 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 9, 2026.

Indications (excerpt from the label)

Use(s) temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itchy, watery eyes sneezing 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 43598-936

What is NDC 43598-936?: 43598-936 is the product NDC for Fexofenadine Hydrochloride, Fexofenadine hydrochloride 60 mg/1 tablet, listed with the FDA by Dr. Reddy's Laboratories Inc.. 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?: Dr. Reddy's Laboratories Inc., NDC labeler code 43598. 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 076502

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

FDA NDC Directory listings under ANDA 076502
Product	Strength	Form · route	Labeler	Product NDC
Allergy Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Rite Aid Corporation	11822-3698
Allergy Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Safeway Inc	21130-784
Allergy Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Family Dollar Stores, Inc.	55319-917
Fexofenadine hydrochloride	Fexofenadine hydrochloride 60 mg/1	TabletOral	Walgreens Company	0363-0783
Fexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	KROGER COMPANY	30142-878
Fexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Dr. Reddy's Laboratories Inc.	43598-809
Fexofenadine hydrochloride	Fexofenadine hydrochloride 30 mg/1	TabletOral	Dr. Reddy's Laboratories Limited	55111-782
Fexofenadine hydrochloride	Fexofenadine hydrochloride 60 mg/1	TabletOral	Dr. Reddy's Laboratories Limited	55111-783
Fexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Dr. Reddy's Laboratories Limited	55111-784
Fexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Dollar General	55910-111
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Chain Drug Marketing Associate	63868-025
Fexofenadine hydrochloride	Fexofenadine hydrochloride 60 mg/1	TabletOral	BluePoint Laboratories	68001-439
Fexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	BluePoint Laboratories	68001-440
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Chain Drug Consortium, LLC	68016-995
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Sam's West Inc.	68196-107
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	CVS Health Corp.	69842-052
Fexofenadine Hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Strategic Sourcing Services, LLC	70677-1009
Non-Drowsy Allergy Relieffexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	TARGET CORPORATION	11673-621
Wal-Fexfexofenadine hydrochloride	Fexofenadine hydrochloride 180 mg/1	TabletOral	Walgreens Company	0363-0784