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NDC 49348-0818-44 Sunmark Loratadine 10 mg/1 Details
Sunmark Loratadine 10 mg/1
Sunmark Loratadine is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Strategic Sourcing Services LLC. 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: 49348-0818-44Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Loratadine
Product Information
| NDC | 49348-0818 |
|---|---|
| Product ID | 49348-818_b14990f8-9e84-4d8a-8e28-a9f2271254f7 |
| Associated GPIs | 41550030000320 |
| 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 | Sunmark 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 | Strategic Sourcing Services LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076301 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 49348-0818-44 (49348081844)
| NDC Package Code | 49348-818-44 |
|---|---|
| Billing NDC | 49348081844 |
| Package | 30 BLISTER PACK in 1 CARTON (49348-818-44) / 1 TABLET in 1 BLISTER PACK |
| Marketing Start Date | 2007-06-21 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |
Standard Product Labeling (SPL)/Prescribing Information SPL d17f1c32-095c-48e9-acc5-d5b94571b9b4 Details
Uses
Warnings
Ask a doctor before use if you have
liver or kidney disease. Your doctor should determine if you need a different dose.
When using this product
do not take more than directed. Taking more than directed may cause drowsiness.
Directions
Other information
Principal Display Panel
COMPARE TO CLARITIN® TABLETS ACTIVE INGREDIENT
24 HOUR
loratadine tablets, 10 mg
Antihistamine
24 hour relief of sneezing; runny nose;
itchy, watery eyes;
itchy throat or nose
Indoor & Outdoor Allergies
ORIGINAL PRESCRIPTION STRENGTH
NON-DROWSY*
Actual Size
*When taken as directed.
See Drug Facts Panel.
GLUTEN FREE
70 TABLETS
INGREDIENTS AND APPEARANCE
| SUNMARK LORATADINE
loratadine tablet |
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| Labeler - Strategic Sourcing Services LLC (116956644) |