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NDC 41250-0724-52 Loratadine and Pseudoephedrine Sulfate 10; 240 mg/1; mg/1 Details

Loratadine and Pseudoephedrine Sulfate 10; 240 mg/1; mg/1

Loratadine and Pseudoephedrine Sulfate is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Meijer Distribution, Inc.. 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: 41250-0724-52
Last Updated: 11/30/2022
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: 41250-0724-52
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Pseudoephedrine

Product Information

NDC	41250-0724
Product ID	41250-724_e1ae1d85-8b3c-4a7a-b174-fcb30c3853c8
Associated GPIs	43993002597520
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Loratadine and Pseudoephedrine Sulfate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Loratadine and Pseudoephedrine Sulfate
Product Type	HUMAN OTC DRUG
Dosage Form	TABLET, FILM COATED, EXTENDED RELEASE
Route	ORAL
Active Ingredient Strength	10; 240
Active Ingredient Units	mg/1; mg/1
Substance Name	LORATADINE; PSEUDOEPHEDRINE SULFATE
Labeler Name	Meijer Distribution, Inc.
Pharmaceutical Class	Adrenergic alpha-Agonists [MoA], alpha-Adrenergic Agonist [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA076557
Listing Certified Through	2024-12-31

Package

NDC 41250-0724-52 (41250072452)

Pricing Information	N/A
NDC Package Code	41250-724-52
Billing NDC	41250072452
Package	15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (41250-724-52)
Marketing Start Date	2004-11-17
NDC Exclude Flag	N