NDC codes

FDA NDC Directory
Product NDC (as listed)0363-0270Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00363-0270Add 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 NDC11-digit (billing)PackageCopy
0363-0270-1000363027010003630270102 BLISTER PACK in 1 CARTON (0363-0270-10) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Aug 27, 2026

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

Generic name (nonproprietary)
fexofenadine hydrochloride and pseudoephedrine hydrochloride
Active ingredients
Fexofenadine hydrochloride — 180 mg/1Pseudoephedrine hydrochloride — 240 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Labeler
WALGREEN CO.NDC labeler code 0363
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215232
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 0363-0270_db9e5d0b-a865-49e7-b5c4-1fc6eb205339SPL ID db9e5d0b-a865-49e7-b5c4-1fc6eb205339SPL set ID 4daddd32-615f-aedf-e063-6394a90a5b09RxCUI 997415UNII 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

N400363027010 followed by a unit qualifier and the quantity

Package 00363-0270-10. 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 .

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 0363-0270

What is NDC 0363-0270?
0363-0270 is the product NDC for Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, Fexofenadine hydrochloride 180 mg/1; Pseudoephedrine hydrochloride 240 mg/1 tablet, film coated, extended release, listed with the FDA by WALGREEN CO.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride.
What is the active ingredient?
Fexofenadine hydrochloride, Pseudoephedrine hydrochloride.
Who is the labeler?
WALGREEN CO., NDC labeler code 0363. 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 and Pseudoephedrine Hydrochloride?
21 other product NDCs are listed under this name. See all Fexofenadine Hydrochloride and Pseudoephedrine 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 and Pseudoephedrine Hydrochloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 180 mg/1; Pseudoephedrine hydrochloride 240 mg/1Tablet, Film coated, Extended releaseOralAurohealth LLC58602-84458602-0844-6058602-0844-6658602-0844-85
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralRugby Laboratories0536-143100536-1431-0700536-1431-34
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralCardinal Health70000-067770000-0677-0170000-0677-02
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralCVS Pharmacy, Inc.51316-00751316-0007-6751316-0007-84
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Extended releaseOralCVS Health Corp51316-01551316-0015-2051316-0015-30
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Extended releaseOralWalgreens Company0363-004400363-0044-2000363-0044-30
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Extended releaseOralRite Aid Corporation11822-002111822-0021-0411822-0021-06
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Extended releaseOralKroger Company30142-09730142-0097-20
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Extended releaseOralStrategic Sourcing Services, LLC70677-101070677-1010-01
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Extended releaseOralWal-mart Stores, Inc.79903-10879903-0108-2079903-0108-30

All 22 Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride NDCs

Other NDCs under ANDA 215232

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

FDA NDC Directory listings under ANDA 215232
ProductStrengthForm · routeLabelerProduct NDC
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 180 mg/1; Pseudoephedrine hydrochloride 240 mg/1Tablet, Film coated, Extended releaseOralAurohealth LLC58602-844

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