NDC codes

FDA NDC Directory
Product NDC (as listed)0536-1431Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00536-1431Add 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
0536-1431-0700536143107005361431073 BLISTER PACK in 1 CARTON (0536-1431-07) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKMarketed from May 17, 2024
0536-1431-3400536143134005361431342 BLISTER PACK in 1 CARTON (0536-1431-34) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACKMarketed from May 17, 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

Generic name (nonproprietary)
fexofenadine hydrochloride and pseudoephedrine hydrochloride
Active ingredients
Fexofenadine hydrochloride — 60 mg/1Pseudoephedrine hydrochloride — 120 mg/1
Dosage form
Tablet, Film coated, Extended release
Route
Oral
Labeler
Rugby LaboratoriesNDC labeler code 0536
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209116
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 0536-1431_cc6df813-9175-4c0b-a8e4-afcaa3aa833fSPL ID cc6df813-9175-4c0b-a8e4-afcaa3aa833fSPL set ID cc6df813-9175-4c0b-a8e4-afcaa3aa833fRxCUI 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

N400536143107 followed by a unit qualifier and the quantity

Package 00536-1431-07. 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 0536-1431

What is NDC 0536-1431?
0536-1431 is the product NDC for Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride, Fexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1 tablet, film coated, extended release, listed with the FDA by Rugby Laboratories. It has 2 package NDCs, 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?
Rugby Laboratories, NDC labeler code 0536. 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 releaseOralWALGREEN CO.0363-027000363-0270-10
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 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 209116

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

FDA NDC Directory listings under ANDA 209116
ProductStrengthForm · routeLabelerProduct NDC
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralWALGREEN CO.0363-0094
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralKROGER COMPANY30142-059
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralCVS Pharmacy, Inc.51316-007
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralAurohealth LLC58602-807
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralCardinal Health70000-0677

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