Search by Drug Name or NDC
NDC 70677-0036-01 sunmark loratadine d 5; 120 mg/1; mg/1 Details
sunmark loratadine d 5; 120 mg/1; mg/1
sunmark loratadine d is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Strategic Sourcing Services LLC. The primary component is LORATADINE; PSEUDOEPHEDRINE SULFATE.
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: 70677-0036-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Loratadine
Pseudoephedrine is used to relieve nasal congestion caused by colds, allergies, and hay fever. It is also used to temporarily relieve sinus congestion and pressure. Pseudoephedrine will relieve symptoms but will not treat the cause of the symptoms or speed recovery. Pseudoephedrine is in a class of medications called nasal decongestants. It works by causing narrowing of the blood vessels in the nasal passages.
Related Packages: 70677-0036-01Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Pseudoephedrine
Product Information
| NDC | 70677-0036 |
|---|---|
| Product ID | 70677-0036_892cf1be-722b-4e30-943a-821b5d754edc |
| Associated GPIs | 43993002597430 |
| GCN Sequence Number | 017181 |
| GCN Sequence Number Description | loratadine/pseudoephedrine TAB ER 12H 5 MG-120MG ORAL |
| HIC3 | Z2O |
| HIC3 Description | 2ND GEN ANTIHISTAMINE AND DECONGESTANT COMBINATION |
| GCN | 63570 |
| HICL Sequence Number | 006605 |
| HICL Sequence Number Description | LORATADINE/PSEUDOEPHEDRINE SULFATE |
| Brand/Generic | Generic |
| Proprietary Name | sunmark loratadine d |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | loratadine, Pseudoephedrine sulfate |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
| Route | ORAL |
| Active Ingredient Strength | 5; 120 |
| Active Ingredient Units | mg/1; mg/1 |
| Substance Name | LORATADINE; PSEUDOEPHEDRINE SULFATE |
| Labeler Name | Strategic Sourcing Services LLC |
| Pharmaceutical Class | Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076050 |
| Listing Certified Through | 2024-12-31 |
Package
Package Images
NDC 70677-0036-01 (70677003601)
| NDC Package Code | 70677-0036-1 |
|---|---|
| Billing NDC | 70677003601 |
| Package | 20 BLISTER PACK in 1 CARTON (70677-0036-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Marketing Start Date | 2018-06-04 |
| NDC Exclude Flag | N |
| Pricing Information | |
| Price Per Unit | 0.84267 |
| Pricing Unit | EA |
| Effective Date | 2024-02-21 |
| NDC Description | SM LORATADINE-D 12 HOUR TABLET |
| Pharmacy Type Indicator | C/I |
| OTC | Y |
| Explanation Code | 1 |
| Classification for Rate Setting | G |
| As of Date | 2024-02-21 |
Standard Product Labeling (SPL)/Prescribing Information SPL 16fe5fc2-3de7-4041-855b-43b1ff902d7b Details
Uses
- •
- temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- •
- sneezing
- •
- itchy, watery eyes
- •
- runny nose
- •
- itching of the nose or throat
- •
- temporarily relieves nasal congestion due to the common cold, hay fever or other upper respiratory allergies
- •
- reduces swelling of nasal passages
- •
- temporarily relieves sinus congestion and pressure
- •
- temporarily restores freer breathing through the nose
Warnings
Do not use
- •
- if you have ever had an allergic reaction to this product or any of its ingredients
- •
- if you are now taking a prescription monoamine oxidase inhibitor (MAOI) (certain drugs for depression, psychiatric, or emotional conditions, or Parkinson’s disease), or for 2 weeks after stopping the MAOI drug. If you do not know if your prescription drug contains an MAOI, ask a doctor or pharmacist before taking this product.
Ask a doctor before use if you have
- •
- heart disease
- •
- thyroid disease
- •
- high blood pressure
- •
- diabetes
- •
- trouble urinating due to an enlarged prostate gland
- •
- 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
Inactive ingredients
Package/Label Principal Display Panel
COMPARE TO CLARITIN-D® 12 HOUR EXTENDED RELEASE TABLETS ACTIVE INGREDIENTS
allergy & congestion
12 HOUR
loratadine D
Pseudoephedrine Sulfate 120 mg/Nasal Decongestant
Loratadine 5 mg/Antihistamine
Extended Release Tablets
Relief of:
nasal & sinus congestion due to colds or allergies
sneezing; runny nose; itchy, watery eyes; itchy throat or nose due to allergies
Indoor & Outdoor Allergies
*When taken as directed. See Drug Facts Panel.
NON-DROWSY*
GLUTEN FREE
Actual Size
20 TABLETS
INGREDIENTS AND APPEARANCE
| SUNMARK LORATADINE D
loratadine, pseudoephedrine sulfate tablet, film coated, extended release |
||||||||||||||||||||
|
||||||||||||||||||||
|
||||||||||||||||||||
|
||||||||||||||||||||
|
||||||||||||||||||||
|
||||||||||||||||||||
|
||||||||||||||||||||
| Labeler - Strategic Sourcing Services LLC (116956644) |