What is NDC 79903-424?

79903-424 is the product NDC for Equate Allergy Relief D, Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1 tablet, film coated, extended release, listed with the FDA by WALMART INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Equate Allergy Relief D (Fexofenadine hydrochloride, pseudoephedrine hydrochloride).

What is the active ingredient?

Fexofenadine hydrochloride, Pseudoephedrine hydrochloride.

WALMART INC., NDC labeler code 79903. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Equate Allergy Relief D?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Equate Allergy Relief D NDC 79903-424

NDC codes

FDA NDC Directory

Product NDC (as listed)79903-424Labeler and product segments. Claims need a package NDC.

Product NDC at billing width79903-0424Add 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
79903-424-20	7990304242079903042420	20 BLISTER PACK in 1 CARTON (79903-424-20) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Aug 6, 2026

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): Equate Allergy Relief D
Generic name (nonproprietary): fexofenadine hydrochloride, pseudoephedrine hydrochloride
Active ingredients: Fexofenadine hydrochloride — 60 mg/1Pseudoephedrine hydrochloride — 120 mg/1
Dosage form: Tablet, Film coated, Extended release
Route: Oral
Labeler: WALMART INC.NDC labeler code 79903
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 216792
Marketing start: Aug 6, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Adrenergic alpha-Agonists (Mechanism)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 79903-424_c78d594a-96c7-40ab-bbbf-51a353df8da1SPL ID c78d594a-96c7-40ab-bbbf-51a353df8da1SPL set ID 6daeb739-a112-4a37-abbb-0bbc41b42df3RxCUI 997406UNII 2S068B75ZU, 6V9V2RYJ8N
Pharmacologic class: Histamine-1 Receptor Antagonist; alpha-Adrenergic Agonist

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

N479903042420 followed by a unit qualifier and the quantity

Package 79903-0424-20. 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 3, 2026.

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 • temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies • reduces swelling of nasal passages • temporarily relieves sinus congestion and pressure • temporarily restores freer breathing through the nose

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 79903-424

What is NDC 79903-424?: 79903-424 is the product NDC for Equate Allergy Relief D, Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1 tablet, film coated, extended release, listed with the FDA by WALMART INC.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Equate Allergy Relief D (Fexofenadine hydrochloride, pseudoephedrine hydrochloride).
What is the active ingredient?: Fexofenadine hydrochloride, Pseudoephedrine hydrochloride.
Who is the labeler?: WALMART INC., NDC labeler code 79903. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Equate Allergy Relief D?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under ANDA 216792

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

FDA NDC Directory listings under ANDA 216792
Product	Strength	Form · route	Labeler	Product NDC
Foster And Thrive Allergy And Congestion Dfexofenadine hydrochloride, pseudoephedrine hydrochloride	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Film coated, Extended releaseOral	Strategic Sourcing Services LLC	70677-1315
Leader 12Hr Allergy And Congestion Relieffexofenadine hydrochloride, pseudoephedrine hydrochloride	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Film coated, Extended releaseOral	Cardinal Health 110, LLC. dba Leader	70000-0772
Rugby Allergy Relief Dfexofenadine hydrochloride, pseudoephedrine hydrochloride	Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1	Tablet, Film coated, Extended releaseOral	Rugby Laboratories	0536-1491