NDC codes

FDA NDC Directory
Product NDC (as listed)66715-9732Labeler and product segments. Claims need a package NDC.
Product NDC at billing width66715-9732Add 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
66715-9732-1667159732011 POUCH in 1 CARTON (66715-9732-1) / 1 TABLET in 1 POUCHMarketed from Mar 1, 2016
66715-9732-2667159732022 POUCH in 1 CARTON (66715-9732-2) / 1 TABLET in 1 POUCHMarketed from Mar 1, 2016

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)
Lil Drug Store Claritin Non-Drowsy, 24 HourSuffix: Non-Drowsy, 24 Hour
Generic name (nonproprietary)
loratadine
Active ingredients
Loratadine — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Over-the-counter drug
Marketing category
NDA — New Drug ApplicationApplication NDA 019658
Marketing start
Listing expires
Identifiers
Product ID 66715-9732_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

N466715973201 followed by a unit qualifier and the quantity

Package 66715-9732-01. 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 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)

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
ProductStrengthForm · routeLabelerProduct NDC
Claritin, BSX Non-Drowsy, 24 HourloratadineLoratadine 10 mg/1TabletOralLil' Drug Store Products, Inc66715-6432
ClaritinloratadineLoratadine 10 mg/1TabletOralBayer HealthCare LLC.11523-4359
Claritin, CVP Non-Drowsy, 24 HourloratadineLoratadine 10 mg/1TabletOralLil' Drug Store Products, Inc66715-6532
ClaritinloratadineLoratadine 10 mg/1TabletOralNavajo Manufacturing Company67751-153
ClaritinloratadineLoratadine 10 mg/1TabletOralNavajo Manufacturing Company Inc.67751-153
ClaritinloratadineLoratadine 10 mg/1TabletOralBayer HealthCare LLC11523-6655
ClaritinloratadineLoratadine 10 mg/1TabletOralBayer HealthCare LLC.11523-7160
ClaritinloratadineLoratadine 10 mg/1TabletOralBayer HealthCare LLC.11523-1527
ClaritinloratadineLoratadine 10 mg/1TabletOralR J General Corporation70264-030
ClaritinloratadineLoratadine 10 mg/1TabletOralBayer HealthCare LLC.11523-7237

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