NDC codes

FDA NDC Directory
Product NDC (as listed)50090-8075Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-8075Add 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
50090-8075-05009080750010 TABLET in 1 BOTTLE (50090-8075-0)Marketed from Sep 16, 2026
50090-8075-45009080750430 TABLET in 1 BOTTLE (50090-8075-4)Marketed from Sep 16, 2026
50090-8075-55009080750590 TABLET in 1 BOTTLE (50090-8075-5)Marketed from Sep 16, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Generic name (nonproprietary)
loratadine
Active ingredients
Loratadine — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214684
Marketing start
Listing expires
Identifiers
Product ID 50090-8075_2777d0aa-200c-44b9-938d-0cca10bd6ae8SPL ID 2777d0aa-200c-44b9-938d-0cca10bd6ae8

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

N450090807500 followed by a unit qualifier and the quantity

Package 50090-8075-00. 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

The FDA listing for this product does not reference a label (SPL) set.

Other NDCs under ANDA 214684

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

FDA NDC Directory listings under ANDA 214684
ProductStrengthForm · routeLabelerProduct NDC
Gencare-Allergy Relief Loratadine Tablets, 10 mgloratadineLoratadine 10 mg/1TabletOralPioneer Life Sciences, LLC72090-051
ValuMeds Allergy Relief LoratadineloratadineLoratadine 10 mg/1TabletOralCabinet Health P.B.C.82725-1142
CVS LoratadineloratadineLoratadine 10 mg/1TabletOralCVS Pharmacy51316-184
LoratadineLoratadine 10 mg/1TabletOralGobrands, Inc82501-1580
LoratadineLoratadine 10 mg/1TabletOralPreferred Pharmaceuticals Inc68788-8616
LoratadineLoratadine 10 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-5308
LoratadineLoratadine 10 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0352
LoratadineLoratadine 10 mg/1TabletOralRising Pharmaceuticals, Inc16571-822
Nuvicare-Allergy Relief Loratadine Tablets, 10 mgloratadineLoratadine 10 mg/1TabletOralNUVICARE LLC84324-027
LoratadineLoratadine 10 mg/1TabletOralStrategic Sourcing Services, LLC70677-1240
LoratadineLoratadine 10 mg/1TabletOralCabinet Health P.B.C.82725-0142

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