NDC codes

FDA NDC Directory
Product NDC (as listed)21130-221Labeler and product segments. Claims need a package NDC.
Product NDC at billing width21130-0221Add 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
21130-221-84211300221843 BLISTER PACK in 1 CARTON (21130-221-84) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Sep 20, 2023

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)
Loratadine ODT
Generic name (nonproprietary)
loratadine
Active ingredients
Loratadine10 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 208477
Marketing start
Listing expires
Identifiers
Product ID 21130-221_57487b79-812f-4626-a068-be397bb1f7fdSPL ID 57487b79-812f-4626-a068-be397bb1f7fdSPL set ID fad93257-bfcf-5e04-e053-6394a90a10a6RxCUI 311373UNII 7AJO3BO7QN

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

N421130022184 followed by a unit qualifier and the quantity

Package 21130-0221-84. 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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 208477

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

FDA NDC Directory listings under ANDA 208477
ProductStrengthForm · routeLabelerProduct NDC
Childrens Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralWALGREEN CO.0363-4020
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralAhold U.S.A., Inc,60000-950
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralWALGREEN CO.0363-9937
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralDISCOUNT DRUG MART53943-035
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralWal-Mart Stores, Inc.49035-806
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralWal-Mart Stores, Inc.49035-806
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralAurohealth LLC58602-744
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralRugby Laboratories0536-1367
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralAmerisource Bergen46122-539
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralAurohealth LLC58602-821
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralAurohealth LLC58602-830
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralCVS Pharmacy, Inc.69842-085
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralAurohealth LLC58602-881
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralChain Drug Consortium, LLC68016-088

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