NDC codes

FDA NDC Directory
Product NDC (as listed)0536-1367Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00536-1367Add 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
0536-1367-07005361367073 BLISTER PACK in 1 CARTON (0536-1367-07) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Oct 6, 2022

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

Brand name (proprietary)
Loratadine ODT
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 208477
Marketing start
Listing expires
Identifiers
Product ID 0536-1367_e4fff55f-aace-428a-b474-e85cfd1fe6f5SPL ID e4fff55f-aace-428a-b474-e85cfd1fe6f5SPL set ID f59f3400-da77-4eb7-be02-842071d87faeRxCUI 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

N400536136707 followed by a unit qualifier and the quantity

Package 00536-1367-07. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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 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 disintegratingOralBetter Living Brands, LLC21130-221
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralAurohealth LLC58602-881
Loratadine ODTloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralChain Drug Consortium, LLC68016-088

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