NDC codes

FDA NDC Directory
Product NDC (as listed)21130-099Labeler and product segments. Claims need a package NDC.
Product NDC at billing width21130-0099Add 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
21130-099-97211300099971 BOTTLE in 1 CARTON (21130-099-97) / 25 CAPSULE in 1 BOTTLEMarketed from Nov 15, 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)
Cetirizine Hydrochloride (Allergy)
Generic name (nonproprietary)
cetirizine hydrochloride
Active ingredients
Cetirizine hydrochloride — 10 mg/1
Dosage form
Capsule
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209107
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 21130-099_b3b261a6-e56a-458a-a5a4-92bd95f4e2fcSPL ID b3b261a6-e56a-458a-a5a4-92bd95f4e2fcSPL set ID f7deb8ca-4a26-aece-e053-6294a90aa685RxCUI 1014675UNII 64O047KTOA
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

N421130009997 followed by a unit qualifier and the quantity

Package 21130-0099-97. 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 209107

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

FDA NDC Directory listings under ANDA 209107
ProductStrengthForm · routeLabelerProduct NDC
Amazon Basics All Day Allergy Reliefcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1CapsuleOralAmazon.com Services LLC72288-013
Cetirizine Hydrochloride (Allergy)cetirizine hydrochlorideCetirizine hydrochloride 10 mg/1CapsuleOralRITE AID CORPORATION11822-4228
Cetirizine Hydrochloride (Allergy)cetirizine hydrochlorideCetirizine hydrochloride 10 mg/1CapsuleOralAurohealth LLC58602-716
Cetirizine Hydrochloride (Hives Relief)cetirizine hydrochlorideCetirizine hydrochloride 10 mg/1CapsuleOralAurohealth LLC58602-808
Cetirizine Hydrochloride (Allergy)cetirizine hydrochlorideCetirizine hydrochloride 10 mg/1CapsuleOralAurohealth LLC58602-806
Cetirizine Hydrochloride (Allergy)cetirizine hydrochlorideCetirizine hydrochloride 10 mg/1CapsuleOralAurohealth LLC58602-863
Cetirizine Hydrochloride (Allergy)cetirizine hydrochlorideCetirizine hydrochloride 10 mg/1CapsuleOralWALGREEN CO.0363-0068

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