NDC codes

FDA NDC Directory
Product NDC (as listed)41415-995Labeler and product segments. Claims need a package NDC.
Product NDC at billing width41415-0995Add 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
41415-995-20414150995201 BLISTER PACK in 1 CARTON (41415-995-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Nov 8, 2021
41415-995-30414150995301 BLISTER PACK in 1 CARTON (41415-995-30) / 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Nov 8, 2021

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)
Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride
Generic name (nonproprietary)
fexofenadine hydrochloride and pseudoephedrine hydrochloride
Active ingredients
Fexofenadine hydrochloride — 60 mg/1Pseudoephedrine hydrochloride — 120 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090818
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha-Agonists (Mechanism)Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 41415-995_aac48a0b-2b28-4c14-9baa-84c08713e6c2SPL ID aac48a0b-2b28-4c14-9baa-84c08713e6c2SPL set ID 75236b23-af51-40b6-ad1b-f62a27093a16RxCUI 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

N441415099520 followed by a unit qualifier and the quantity

Package 41415-0995-20. 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 .

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)

Other NDCs under ANDA 090818

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

FDA NDC Directory listings under ANDA 090818
ProductStrengthForm · routeLabelerProduct NDC
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralAmeriSource Bergen46122-694
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralOhm Laboratories Inc.51660-037
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralH E B37808-999
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralwalgreens0363-2110
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralSun Pharmaceutical Industries, Inc.47335-724
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Extended releaseOralCVS Pharmacy69842-973
Fexofenadine Hydrochloride and Pseudoephedrine HydrochlorideFexofenadine hydrochloride 60 mg/1; Pseudoephedrine hydrochloride 120 mg/1Tablet, Film coated, Extended releaseOralCVS Pharmacy69842-990

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