Over-the-counter drug · ANDA

Allergy (Cetirizine hydrochloride) NDC 41226-692

Cetirizine hydrochloride 10 mg/1 · Tablet, Film coated · Oral · Kroger Company

NDC codes

FDA NDC Directory
Product NDC (as listed)41226-692Labeler and product segments. Claims need a package NDC.
Product NDC at billing width41226-0692Add 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
41226-692-1441226069214412260692142 BOTTLE in 1 CARTON (41226-692-14) / 70 TABLET, FILM COATED in 1 BOTTLEMarketed from May 11, 2021
41226-692-6541226069265412260692651 BOTTLE in 1 CARTON (41226-692-65) / 365 TABLET, FILM COATED in 1 BOTTLEMarketed from May 11, 2021
41226-692-7041226069270412260692701 BOTTLE in 1 CARTON (41226-692-70) / 70 TABLET, FILM COATED in 1 BOTTLEMarketed from Jun 3, 2024

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)
Allergy
Generic name (nonproprietary)
cetirizine hydrochloride
Active ingredients
Cetirizine hydrochloride — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Kroger CompanyNDC labeler code 41226
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078933
Marketing start
Listing expires
Other FDA classes
Histamine H1 Receptor Antagonists (Mechanism)
Identifiers
Product ID 41226-692_3e7fad54-62e1-6d0a-e063-6394a90a5785SPL ID 3e7fad54-62e1-6d0a-e063-6394a90a5785SPL set ID bc020340-ef39-e49a-e053-2a95a90af810RxCUI 1014678UNII 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

N441226069214 followed by a unit qualifier and the quantity

Package 41226-0692-14. 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 sneezing itchy, watery eyes 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 41226-692

What is NDC 41226-692?
41226-692 is the product NDC for Allergy (cetirizine hydrochloride), Cetirizine hydrochloride 10 mg/1 tablet, film coated, listed with the FDA by Kroger Company. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Allergy (Cetirizine hydrochloride).
What is the active ingredient?
Cetirizine hydrochloride.
Who is the labeler?
Kroger Company, NDC labeler code 41226. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Allergy?
25 other product NDCs are listed under this name. See all Allergy 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 Allergy NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Allergymometasone furoateMometasone furoate monohydrate 50 ug/1Spray, MeteredNasalAmazon.com Services LLC72288-50672288-0506-02
Allergyfexofenadine hydrochlorideFexofenadine hydrochloride 180 mg/1Tablet, Film coatedOralAmazon.com Services LLC72288-71672288-0716-0072288-0716-39
allergymometasone furoate monohydrateMometasone furoate monohydrate 50 ug/1Spray, MeteredNasalHyVee Inc42507-18242507-0182-02
Allergydiphenhydramine hclDiphenhydramine hydrochloride 25 mg/1Tablet, Film coatedOralPublix Super Markets Inc56062-92356062-0923-0856062-0923-12
Allergymometasone furoate monohydrateMometasone furoate monohydrate 50 ug/1Spray, MeteredNasalRite Aid Corporation11822-709911822-7099-01
allergymometasone furoate monohydrateMometasone furoate monohydrate 50 ug/1Spray, MeteredNasalCVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED51316-11751316-0117-11
Allergyallium cepa, ambrosia, arsenicum alb, carbo veg, euphrasia, nux vom, phosphorus, pulsatilla, sulphur, solidagoOnion 30 [hp_C]/mL + 8 more ingredientsLiquidOralZorex International81825-000781825-0007-01
Allergydiphenhydramine hydrochlorideDiphenhydramine hydrochloride 25 mg/1Tablet, Film coatedOralKroger Company41226-16041226-0160-0141226-0160-4041226-0160-42
Allergyallium sat, anacardium, apis mel, gambogia, merc solub, nat carb, nitricum ac, nux vom, phosphorus, pulsatilla, sulphurGarlic 12 [hp_X]/59.1mL + 10 more ingredientsLiquidOralNet Remedies61626-010961626-0109-04
Allergydiphenhydramine hydrochlorideDiphenhydramine hydrochloride 25 mg/1TabletOralVelocity Pharma LLC76168-12176168-0121-12

All 26 Allergy NDCs

Other NDCs under ANDA 078933

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

FDA NDC Directory listings under ANDA 078933
ProductStrengthForm · routeLabelerProduct NDC
All Day Allergy Reliefcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralDOLGENCORP, INC.55910-269
Allergy Reliefcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralWALGREENS0363-1794
Allergy Reliefcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralBETTER LIVING BRANDS, LLC21130-712
Cetirizine HydrochlorideCetirizine hydrochloride 5 mg/1TabletOralTIME CAP LABORATORIES, INC.49483-682
Cetirizine Hydrochloride Tablets, 10 mgcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralMARKSANS PHARMA LIMITED25000-220
Cetirizine Hydrochloride Tablets, 10 mg (Oval Shape)cetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralMARKSANS PHARMA LIMITED25000-160
Cetirizine Hydrochloride Tablets, 5 mgcetirizine hydrochlorideCetirizine hydrochloride 5 mg/1TabletOralMARKSANS PHARMA LIMITED25000-219
Cetirizine Hydrochloride Tablets,10 mgcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralTIME CAP LABORATORIES, INC.49483-692
Cetirizine Hydrochloride Tablets,10 mgcetirizine hydrochlorideCetirizine hydrochloride 10 mg/1TabletOralNorthwind Health Company, LLC51655-842

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