Over-the-counter drug · NDA
Zyrtec Allergy (cetirizine hydrochloride) NDC 85237-2960
Cetirizine hydrochloride 10 mg/1 · Tablet, Film coated · Oral · Select Consumer Group
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 85237-2960-1 | 85237296001 | 1 POUCH in 1 BLISTER PACK (85237-2960-1) / 1 TABLET, FILM COATED in 1 POUCH (85237-2960-0)Marketed from Jan 1, 2008 | |
| 85237-2960-3 | 85237296003 | 20 POUCH in 1 CARTON (85237-2960-3) / 1 TABLET, FILM COATED in 1 POUCH (85237-2960-0)Marketed from Jan 1, 2008 |
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)
- Zyrtec Allergy
- Generic name (nonproprietary)
- cetirizine hydrochloride
- Active ingredients
- Cetirizine hydrochloride — 10 mg/1
- Dosage form
- Tablet, Film coated
- Route
- Oral
- Labeler
- Select Consumer Group
- Product type
- Over-the-counter drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 019835
- Marketing start
- Listing expires
- Other FDA classes
- Histamine H1 Receptor Antagonists (Mechanism)
- Identifiers
- Product ID 85237-2960_568960cf-2c90-f1b0-e063-6294a90aebc7SPL ID 568960cf-2c90-f1b0-e063-6294a90aebc7SPL set ID 568960cf-2c8f-f1b0-e063-6294a90aebc7RxCUI 1014678, 1020026UNII 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
N485237296001followed by a unit qualifier and the quantityPackage 85237-2960-01. 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.
Other NDCs under NDA 019835
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 |
|---|---|---|---|---|
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Morning Star OTC | 53209-5001 |
| ZYRTEC Hivescetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Kenvue Brands LLC | 50580-116 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Navajo Manufacturing Company Incorporated | 67751-192 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Kenvue Brands LLC | 50580-726 |
| Zyrtec Allergycetirizine hydrochloride | — | Kit | Kenvue Brands LLC | 50580-752 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 5 mg/1 | Tablet, Film coatedOral | Kenvue Brands LLC | 50580-754 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Savings Distributors LLC | 73097-016 |
| Zyrtec Allergycetirizine hydrochloride | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | RedPharm Drug Inc | 67296-1484 |
| Zyrtec Allergy, Lil Drug Storecetirizine hydrochloride tablet, film coated | Cetirizine hydrochloride 10 mg/1 | Tablet, Film coatedOral | Lil' Drug Store Products, Inc. | 66715-9811 |