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| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 41226-692-14 | 41226069214 | 2 BOTTLE in 1 CARTON (41226-692-14) / 70 TABLET, FILM COATED in 1 BOTTLEMarketed from May 11, 2021 | |
| 41226-692-65 | 41226069265 | 1 BOTTLE in 1 CARTON (41226-692-65) / 365 TABLET, FILM COATED in 1 BOTTLEMarketed from May 11, 2021 | |
| 41226-692-70 | 41226069270 | 1 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 Company
- 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
N441226069214followed by a unit qualifier and the quantityPackage 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
Label details couldn’t be retrieved right now. Open the label on DailyMed.
Other NDCs under ANDA 078933
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Allergy Reliefcetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | TabletOral | BETTER LIVING BRANDS, LLC | 21130-712 |
| Allergy Reliefcetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | TabletOral | WALGREENS | 0363-1794 |
| Cetirizine Hydrochloride Tablets, 10 mg (Oval Shape)cetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | TabletOral | MARKSANS PHARMA LIMITED | 25000-160 |
| Cetirizine Hydrochloride Tablets, 5 mgcetirizine hydrochloride | Cetirizine hydrochloride 5 mg/1 | TabletOral | MARKSANS PHARMA LIMITED | 25000-219 |
| Cetirizine Hydrochloride Tablets, 10 mgcetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | TabletOral | MARKSANS PHARMA LIMITED | 25000-220 |
| Cetirizine Hydrochloride Tablets,10 mgcetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | TabletOral | Northwind Health Company, LLC | 51655-842 |
| All Day Allergy Reliefcetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | TabletOral | DOLGENCORP, INC. | 55910-269 |
| Cetirizine Hydrochloride | Cetirizine hydrochloride 5 mg/1 | TabletOral | TIME CAP LABORATORIES, INC. | 49483-682 |
| Cetirizine Hydrochloride Tablets,10 mgcetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | TabletOral | TIME CAP LABORATORIES, INC. | 49483-692 |