NDC codes

FDA NDC Directory
Product NDC (as listed)66715-8815Labeler and product segments. Claims need a package NDC.
Product NDC at billing width66715-8815Add 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
66715-8815-666715881506667158815061 BLISTER PACK in 1 CARTON (66715-8815-6) / 6 TABLET in 1 BLISTER PACKMarketed from May 6, 2022

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)
Non-Drowsy Allergy Relief
Generic name (nonproprietary)
loratadine tablet
Active ingredients
Loratadine — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Lil' Drug Store Products, Inc.NDC labeler code 66715
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076471
Marketing start
Listing expires
Identifiers
Product ID 66715-8815_031fc3e5-b5ec-447c-e063-6294a90a13b5SPL ID 031fc3e5-b5ec-447c-e063-6294a90a13b5SPL set ID 031fc3e5-b5eb-447c-e063-6294a90a13b5RxCUI 311372UNII 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

N466715881506 followed by a unit qualifier and the quantity

Package 66715-8815-06. 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.

About NDC 66715-8815

What is NDC 66715-8815?
66715-8815 is the product NDC for Non-Drowsy Allergy Relief (loratadine tablet), Loratadine 10 mg/1 tablet, listed with the FDA by Lil' Drug Store Products, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Non-Drowsy Allergy Relief (Loratadine tablet).
What is the active ingredient?
Loratadine.
Who is the labeler?
Lil' Drug Store Products, Inc., NDC labeler code 66715. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Non-Drowsy Allergy Relief?
2 other product NDCs are listed under this name. See all Non-Drowsy Allergy Relief 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 Non-Drowsy Allergy Relief NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Non-Drowsy Allergy Relieffexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1TabletOralTARGET CORPORATION11673-62111673-0621-0111673-0621-1511673-0621-30+2 more
non drowsy allergy reliefloratadineLoratadine 10 mg/1Tablet, Orally disintegratingOralMeijer Distribution Inc41250-89041250-0890-65

Other NDCs under ANDA 076471

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

FDA NDC Directory listings under ANDA 076471
ProductStrengthForm · routeLabelerProduct NDC
AllergyloratadineLoratadine 10 mg/1TabletOralSelder, S.A. de C.V.63654-309
Allergy ReliefloratadineLoratadine 10 mg/1TabletOralAllegiant Health69168-309

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