Childrens Fexofenadine Hydrochloride Allergy NDC 0363-2141

NDC codes

FDA NDC Directory

Product NDC (as listed)0363-2141Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00363-2141Add 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
0363-2141-01	00363214101	1 BOTTLE in 1 CARTON (0363-2141-01) / 240 mL in 1 BOTTLEMarketed from Dec 6, 2024
0363-2141-08	00363214108	1 BOTTLE in 1 CARTON (0363-2141-08) / 120 mL in 1 BOTTLEMarketed from Dec 6, 2024

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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: Walgreens Company
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 0363-2141_374f99cb-1562-7532-e063-6394a90a95b4SPL ID 374f99cb-1562-7532-e063-6394a90a95b4SPL set ID 374f9271-b65b-69a9-e063-6394a90af36aRxCUI 997491UNII 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

N400363214101 followed by a unit qualifier and the quantity

Package 00363-2141-01. 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 Jun 11, 2025.

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	Wal-Mart Stores Inc	79903-306
Childrens Fexofenadine Hydrochloride Allergyfexofenadine hydrochloride	Fexofenadine hydrochloride 30 mg/5mL	SuspensionOral	Sun Pharmaceutical Industries, Inc.	51672-2141