Childrens Fexofenadine Hydrochloride Allergy NDC 79903-306

NDC codes

FDA NDC Directory

Product NDC (as listed)79903-306Labeler and product segments. Claims need a package NDC.

Product NDC at billing width79903-0306Add 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
79903-306-04	79903030604	1 BOTTLE in 1 CARTON (79903-306-04) / 120 mL in 1 BOTTLEMarketed from Dec 6, 2024

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): Childrens Fexofenadine Hydrochloride AllergySuffix: Allergy
Generic name (nonproprietary): fexofenadine hydrochloride
Active ingredients: Fexofenadine hydrochloride — 30 mg/5mL
Dosage form: Suspension
Route: Oral
Labeler: Wal-Mart Stores Inc
Product type: Over-the-counter drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208123
Marketing start: Dec 6, 2024
Listing expires: Dec 31, 2026
Other FDA classes: Histamine H1 Receptor Antagonists (Mechanism)
Identifiers: Product ID 79903-306_2905c49e-1ab8-3d84-e063-6394a90ac1a4SPL ID 2905c49e-1ab8-3d84-e063-6394a90ac1a4SPL set ID 2432f862-6d7e-666d-e063-6294a90acf74RxCUI 997491UNII 2S068B75ZUUPC 0194346377169
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

N479903030604 followed by a unit qualifier and the quantity

Package 79903-0306-04. 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 6, 2024.

Indications (excerpt from the label)

Uses 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)

Other NDCs under ANDA 208123

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

FDA NDC Directory listings under ANDA 208123
Product	Strength	Form · route	Labeler	Product NDC
Childrens Fexofenadine Hydrochloride Allergyfexofenadine hydrochloride	Fexofenadine hydrochloride 30 mg/5mL	SuspensionOral	Sun Pharmaceutical Industries, Inc.	51672-2141
Childrens Fexofenadine Hydrochloride Allergyfexofenadine hydrochloride	Fexofenadine hydrochloride 30 mg/5mL	SuspensionOral	Walgreens Company	0363-2141