What is NDC 66715-6432?

66715-6432 is the product NDC for Claritin, BSX Non-Drowsy, 24 Hour, 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?

Claritin, BSX Non-Drowsy, 24 Hour (Loratadine).

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 Claritin, BSX Non-Drowsy, 24 Hour?

None: this is the only finished product listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Claritin, BSX Non-Drowsy, 24 Hour NDC 66715-6432

NDC codes

FDA NDC Directory

Product NDC (as listed)66715-6432Labeler and product segments. Claims need a package NDC.

Product NDC at billing width66715-6432Add 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 NDC	11-digit (billing)	Package	Copy
66715-6432-2	6671564320266715643202	2 POUCH in 1 CARTON (66715-6432-2) / 1 TABLET in 1 POUCHMarketed from Nov 3, 2020

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): Claritin, BSX Non-Drowsy, 24 HourSuffix: Non-Drowsy, 24 Hour
Generic name (nonproprietary): loratadine
Active ingredients: Loratadine — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Lil' Drug Store Products, IncNDC labeler code 66715
Product type: Over-the-counter drug
Marketing category: NDA — New Drug ApplicationApplication NDA 019658
Marketing start: Nov 3, 2020
Listing expires: Dec 31, 2026
Identifiers: Product ID 66715-6432_f71dd792-11e7-0bfd-e053-6294a90ab948SPL ID f71dd792-11e7-0bfd-e053-6294a90ab948SPL set ID f85b0527-107c-4a4a-aad7-61d2f52bad63RxCUI 206805, 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

N466715643202 followed by a unit qualifier and the quantity

Package 66715-6432-02. 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 Mar 17, 2023.

Indications (excerpt from the label)

Uses 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 66715-6432

What is NDC 66715-6432?: 66715-6432 is the product NDC for Claritin, BSX Non-Drowsy, 24 Hour, 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?: Claritin, BSX Non-Drowsy, 24 Hour (Loratadine).
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 Claritin, BSX Non-Drowsy, 24 Hour?: None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under NDA 019658

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

FDA NDC Directory listings under NDA 019658
Product	Strength	Form · route	Labeler	Product NDC
Claritinloratadine	Loratadine 10 mg/1	TabletOral	R J General Corporation	70264-030
Lil Drug Store Claritin Non-Drowsy, 24 Hourloratadine	Loratadine 10 mg/1	TabletOral	Lil' Drug Store Products, Inc	66715-9732
Claritinloratadine	Loratadine 10 mg/1	TabletOral	Bayer HealthCare LLC.	11523-4359
Claritinloratadine	Loratadine 10 mg/1	TabletOral	Bayer HealthCare LLC	11523-6655
Claritinloratadine	Loratadine 10 mg/1	TabletOral	Bayer HealthCare LLC.	11523-1527
Claritinloratadine	Loratadine 10 mg/1	TabletOral	Bayer HealthCare LLC.	11523-7160
Claritinloratadine	Loratadine 10 mg/1	TabletOral	Navajo Manufacturing Company	67751-153
Claritinloratadine	Loratadine 10 mg/1	TabletOral	Navajo Manufacturing Company Inc.	67751-153
Claritinloratadine	Loratadine 10 mg/1	TabletOral	Bayer HealthCare LLC.	11523-7237
Claritin, CVP Non-Drowsy, 24 Hourloratadine	Loratadine 10 mg/1	TabletOral	Lil' Drug Store Products, Inc	66715-6532

Claritin, BSX Non-Drowsy, 24 Hour (Loratadine) NDC 66715-6432