NDC codes

FDA NDC Directory
Product NDC (as listed)16571-822Labeler and product segments. Claims need a package NDC.
Product NDC at billing width16571-0822Add 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
16571-822-011657108220116571082201100 TABLET in 1 BOTTLE (16571-822-01)Marketed from Mar 10, 2022
16571-822-03165710822031657108220330 TABLET in 1 BOTTLE (16571-822-03)Marketed from Mar 10, 2022
16571-822-301657108223016571082230300 TABLET in 1 BOTTLE (16571-822-30)Marketed from Mar 10, 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)
Loratadine
Generic name (nonproprietary)
loratadine
Active ingredients
Loratadine — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Rising Pharmaceuticals, IncNDC labeler code 16571
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214684
Marketing start
Listing expires
Identifiers
Product ID 16571-822_8b088034-c702-4b88-b4e3-421aa9739ec8SPL ID 8b088034-c702-4b88-b4e3-421aa9739ec8SPL set ID d28128a3-af54-440e-9bd4-0fccf393d18aRxCUI 311372UNII 7AJO3BO7QNUPC 0316571822010, 0316571822034

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

N416571082201 followed by a unit qualifier and the quantity

Package 16571-0822-01. 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 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)

About NDC 16571-822

What is NDC 16571-822?
16571-822 is the product NDC for Loratadine, Loratadine 10 mg/1 tablet, listed with the FDA by Rising Pharmaceuticals, Inc. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Loratadine.
What is the active ingredient?
Loratadine.
Who is the labeler?
Rising Pharmaceuticals, Inc, NDC labeler code 16571. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Loratadine?
109 other product NDCs are listed under this name. See all Loratadine NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Loratadine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LoratadineLoratadine 10 mg/1TabletOralYYBA CORP73581-22973581-0229-0173581-0229-03
LoratadineLoratadine 10 mg/1TabletOralAvPAK50268-77750268-0777-01
LoratadineLoratadine 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-410368788-4103-0068788-4103-0168788-4103-03+2 more
LoratadineLoratadine 10 mg/1TabletOralSafecor Health, LLC48433-06448433-0064-20
LoratadineLoratadine 10 mg/1TabletOralAurobindo Pharma Limited84386-11984386-0119-78
LoratadineLoratadine 10 mg/1TabletOralCabinet Health P.B.C.82725-014282725-0142-0182725-0142-0282725-0142-03+1 more
LoratadineLoratadine 10 mg/1TabletOralCardinal Health 107, LLC55154-018855154-0188-00
LoratadineLoratadine 10 mg/1TabletOralMajor Pharmaceuticals0904-751100904-7511-61
LoratadineLoratadine 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-865968788-8659-0068788-8659-0168788-8659-03+2 more
LoratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralTenshi Kaizen Pvt Ltd72983-50372983-0503-06

All 110 Loratadine NDCs

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
CVS LoratadineloratadineLoratadine 10 mg/1TabletOralCVS Pharmacy51316-184
Gencare-Allergy Relief Loratadine Tablets, 10 mgloratadineLoratadine 10 mg/1TabletOralPioneer Life Sciences, LLC72090-051
LoratadineLoratadine 10 mg/1TabletOralA-S Medication Solutions50090-8075
LoratadineLoratadine 10 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-5308
LoratadineLoratadine 10 mg/1TabletOralPreferred Pharmaceuticals Inc68788-8616
LoratadineLoratadine 10 mg/1TabletOralStrategic Sourcing Services, LLC70677-1240
LoratadineLoratadine 10 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0352
LoratadineLoratadine 10 mg/1TabletOralGobrands, Inc82501-1580
LoratadineLoratadine 10 mg/1TabletOralCabinet Health P.B.C.82725-0142
Nuvicare-Allergy Relief Loratadine Tablets, 10 mgloratadineLoratadine 10 mg/1TabletOralNUVICARE LLC84324-027
ValuMeds Allergy Relief LoratadineloratadineLoratadine 10 mg/1TabletOralCabinet Health P.B.C.82725-1142

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