NDC codes

FDA NDC Directory
Product NDC (as listed)57483-950Labeler and product segments. Claims need a package NDC.
Product NDC at billing width57483-0950Add 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
57483-950-10574830950103 BLISTER PACK in 1 CARTON (57483-950-10) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from May 30, 2022

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)
Allervarx
Generic name (nonproprietary)
loratadine
Active ingredients
Loratadine — 10 mg/1
Dosage form
Tablet, Orally disintegrating
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213294
Marketing start
Listing expires
Identifiers
Product ID 57483-950_d91b9ee4-dbd2-459c-a789-a59b7bf61d0eSPL ID d91b9ee4-dbd2-459c-a789-a59b7bf61d0eSPL set ID 885e81ae-5ea3-4d14-8666-8c2698767014RxCUI 311373UNII 7AJO3BO7QNUPC 0357483002329

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

N457483095010 followed by a unit qualifier and the quantity

Package 57483-0950-10. 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 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 213294

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

FDA NDC Directory listings under ANDA 213294
ProductStrengthForm · routeLabelerProduct NDC
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralStrides Pharma Inc59556-917
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralTenshi Kaizen Pvt Ltd72983-501
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralTenshi Kaizen Pvt Ltd72983-503
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralCVS PHARMACY, INC51316-503
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralDr. Reddy's Laboratories Inc.43598-707
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralDr. Reddy's Laboratories Inc.43598-758
Alavert AllergyloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralFoundation Consumer Healthcare69536-190
Alavert AllergyloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralFoundation Consumer Healthcare69536-195

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