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NDC 69848-0019-10 Loratadine 10 mg/1 Details
Loratadine 10 mg/1
Loratadine is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by GRANULES USA, INC.. The primary component is LORATADINE.
MedlinePlus Drug Summary
Loratadine is used to temporarily relieve the symptoms of hay fever (allergy to pollen, dust, or other substances in the air) and other allergies. These symptoms include sneezing, runny nose, and itchy eyes, nose, or throat. Loratadine is also used to treat itching and redness caused by hives. However, loratadine does not prevent hives or other allergic skin reactions. Loratadine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms. Loratadine is also available in combination with pseudoephedrine (Sudafed, others). This monograph only includes information about the use of loratadine alone. If you are taking the loratadine and pseudoephedrine combination product, read the information on the package label or ask your doctor or pharmacist for more information.
Related Packages: 69848-0019-10Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Loratadine
Product Information
| NDC | 69848-0019 |
|---|---|
| Product ID | 69848-019_0cccbfd2-0ed3-2335-e063-6294a90a47e4 |
| Associated GPIs | |
| GCN Sequence Number | 018698 |
| GCN Sequence Number Description | loratadine TABLET 10 MG ORAL |
| HIC3 | Z2Q |
| HIC3 Description | ANTIHISTAMINES - 2ND GENERATION |
| GCN | 60563 |
| HICL Sequence Number | 007605 |
| HICL Sequence Number Description | LORATADINE |
| Brand/Generic | Generic |
| Proprietary Name | Loratadine |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Loratadine |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 10 |
| Active Ingredient Units | mg/1 |
| Substance Name | LORATADINE |
| Labeler Name | GRANULES USA, INC. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA210722 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 69848-0019-10 (69848001910)
| NDC Package Code | 69848-019-10 |
|---|---|
| Billing NDC | 69848001910 |
| Package | 100 TABLET in 1 BOTTLE (69848-019-10) |
| Marketing Start Date | 2021-07-26 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |