Over-the-counter drug · ANDA
All Day Allergy Relief (cetirizine hydrochloride) NDC 55910-269
Cetirizine hydrochloride 10 mg/1 · Tablet · Oral · DOLGENCORP, INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 55910-269-58 | 55910026958 | 1 BOTTLE in 1 CARTON (55910-269-58) / 45 TABLET in 1 BOTTLEMarketed from Dec 20, 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)
- All Day Allergy Relief
- Generic name (nonproprietary)
- cetirizine hydrochloride
- Active ingredients
- Cetirizine hydrochloride — 10 mg/1
- Dosage form
- Tablet
- Route
- Oral
- Labeler
- DOLGENCORP, INC.
- 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 55910-269_0c774d83-58dd-d9b3-e063-6394a90a6f7aSPL ID 0c774d83-58dd-d9b3-e063-6394a90a6f7aSPL set ID 0643ea78-9709-8526-e063-6394a90a227bRxCUI 1014678UNII 64O047KTOAUPC 0355910269581
- 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
N455910026958followed by a unit qualifier and the quantityPackage 55910-0269-58. 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 |
| Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Kroger Company | 41226-692 |
| 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 |