NDC codes

FDA NDC Directory
Product NDC (as listed)69230-323Labeler and product segments. Claims need a package NDC.
Product NDC at billing width69230-0323Add 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
69230-323-01692300323016923003230110 BLISTER PACK in 1 CARTON (69230-323-01) / 10 TABLET in 1 BLISTER PACK (69230-323-32)Marketed from Jul 28, 2023
69230-323-1069230032310692300323101000 TABLET in 1 BOTTLE (69230-323-10)Marketed from Jul 28, 2023
69230-323-3069230032330692300323301 BOTTLE in 1 CARTON (69230-323-30) / 30 TABLET in 1 BOTTLEMarketed from Jul 28, 2023
69230-323-3169230032331692300323311 BOTTLE in 1 CARTON (69230-323-31) / 108 TABLET in 1 BOTTLEMarketed from Jul 28, 2023
69230-323-3369230032333692300323331 BOTTLE in 1 CARTON (69230-323-33) / 100 TABLET in 1 BOTTLEMarketed from Jul 28, 2023
69230-323-3469230032334692300323341 BOTTLE in 1 CARTON (69230-323-34) / 300 TABLET in 1 BOTTLEMarketed from Jul 28, 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
Generic name (nonproprietary)
loratadine
Active ingredients
Loratadine — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Camber Consumer Care IncNDC labeler code 69230
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211718
Marketing start
Listing expires
Identifiers
Product ID 69230-323_04d9c5a8-1f42-f7c0-e063-6294a90a92aeSPL ID 04d9c5a8-1f42-f7c0-e063-6294a90a92aeSPL set ID d57da4bd-af37-414a-a50c-e80d2bb28314RxCUI 311372UNII 7AJO3BO7QNUPC 0369230323342, 0369230323335, 0369230323304

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

N469230032301 followed by a unit qualifier and the quantity

Package 69230-0323-01. 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)

USE(S) 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)

About NDC 69230-323

What is NDC 69230-323?
69230-323 is the product NDC for Loratadine, Loratadine 10 mg/1 tablet, listed with the FDA by Camber Consumer Care Inc. It has 6 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?
Camber Consumer Care Inc, NDC labeler code 69230. 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 211718

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

FDA NDC Directory listings under ANDA 211718
ProductStrengthForm · routeLabelerProduct NDC
LoratadineLoratadine 10 mg/1TabletOralAvPAK50268-777
LoratadineLoratadine 10 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8605
LoratadineLoratadine 10 mg/1TabletOralBryant Ranch Prepack71335-2391
LoratadineLoratadine 10 mg/1TabletOralBryant Ranch Prepack71335-2551
Loratadine 10mgLoratadine 10 mg/1TabletOralAllegiant Health69168-475

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