NDC codes

FDA NDC Directory
Product NDC (as listed)68071-2406Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68071-2406Add 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
68071-2406-96807124060990 TABLET in 1 BOTTLE (68071-2406-9)Marketed from May 21, 2021

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)
levocetirizine dihydrochloride
Generic name (nonproprietary)
levocetirizine dihydrochloride
Active ingredients
Levocetirizine dihydrochloride — 5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203646
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 68071-2406_4ddbe480-0743-9868-e063-6294a90ac953SPL ID 4ddbe480-0743-9868-e063-6294a90ac953SPL set ID c2dbf151-5b3d-5dfb-e053-2995a90a4c19RxCUI 855172UNII SOD6A38AGAUPC 0368071240696
Pharmacologic class
Histamine-1 Receptor Antagonist

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

N468071240609 followed by a unit qualifier and the quantity

Package 68071-2406-09. 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.

Other NDCs under ANDA 203646

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

FDA NDC Directory listings under ANDA 203646
ProductStrengthForm · routeLabelerProduct NDC
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralGolden State Medical Supply, Inc.51407-892
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-7934
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralBryant Ranch Prepack71335-0940
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralProficient Rx LP63187-663
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralScieGen Pharmaceuticals, Inc.50228-136
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralBryant Ranch Prepack63629-8500
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralNorthwind Health Company, LLC51655-564
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8565
Levocetirizine DihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralProficient Rx LP71205-988
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralVensun Pharmaceuticals, Inc.42543-712
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralBryant Ranch Prepack72162-1525
Levocetirizine DihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralProficient Rx LP71205-476
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralBryant Ranch Prepack71335-1952
levocetirizine dihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralBryant Ranch Prepack71335-2283
Levocetirizine DihydrochlorideLevocetirizine dihydrochloride 5 mg/1TabletOralWestminster Pharmaceuticals, LLC69367-238

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