Over-the-counter drug · ANDA
Alavert Allergy (loratadine) NDC 69536-195
Loratadine 10 mg/1 · Tablet, Orally disintegrating · Oral · Foundation Consumer Healthcare
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 69536-195-20 | 69536019520 | 20 BLISTER PACK in 1 CARTON (69536-195-20) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Oct 31, 2024 | |
| 69536-195-60 | 69536019560 | 60 BLISTER PACK in 1 CARTON (69536-195-60) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Oct 31, 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)
- Alavert AllergySuffix: Allergy
- Generic name (nonproprietary)
- loratadine
- Active ingredients
- Loratadine — 10 mg/1
- Dosage form
- Tablet, Orally disintegrating
- Route
- Oral
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 213294
- Marketing start
- Listing expires
- Identifiers
- Product ID 69536-195_1ba62e9b-1b1f-016a-e063-6394a90a065eSPL ID 1ba62e9b-1b1f-016a-e063-6394a90a065eSPL set ID 1704474a-9b99-de45-e063-6294a90ac59bRxCUI 311373, 351855UNII 7AJO3BO7QN
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
N469536019520followed by a unit qualifier and the quantityPackage 69536-0195-20. 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 ANDA 213294
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 |
|---|---|---|---|---|
| Loratadine | Loratadine 10 mg/1 | Tablet, Orally disintegratingOral | Strides Pharma Inc | 59556-917 |
| Allervarxloratadine | Loratadine 10 mg/1 | Tablet, Orally disintegratingOral | Innovus Pharmaceuticals, Inc. | 57483-950 |
| Loratadine | Loratadine 10 mg/1 | Tablet, Orally disintegratingOral | Tenshi Kaizen Pvt Ltd | 72983-501 |
| Loratadine | Loratadine 10 mg/1 | Tablet, Orally disintegratingOral | Tenshi Kaizen Pvt Ltd | 72983-503 |
| Loratadine | Loratadine 10 mg/1 | Tablet, Orally disintegratingOral | CVS PHARMACY, INC | 51316-503 |
| Loratadine | Loratadine 10 mg/1 | Tablet, Orally disintegratingOral | Dr. Reddy's Laboratories Inc. | 43598-707 |
| Loratadine | Loratadine 10 mg/1 | Tablet, Orally disintegratingOral | Dr. Reddy's Laboratories Inc. | 43598-758 |
| Alavert Allergyloratadine | Loratadine 10 mg/1 | Tablet, Orally disintegratingOral | Foundation Consumer Healthcare | 69536-190 |