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NDC 73581-0230-01 LORATADINE ALLERGY RELIEF 10 mg/1 Details

LORATADINE ALLERGY RELIEF 10 mg/1

LORATADINE ALLERGY RELIEF is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by YYBA CORP. 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: 73581-0230-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Loratadine

Product Information

NDC	73581-0230
Product ID	73581-230_0e135981-fabe-f255-e063-6394a90ae356
Associated GPIs
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 ALLERGY RELIEF
Proprietary Name Suffix	10mg
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	YYBA CORP
Pharmaceutical Class	n/a
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA210722
Listing Certified Through	2025-12-31

Package

NDC 73581-0230-01 (73581023001)

Pricing Information	N/A
NDC Package Code	73581-230-01
Billing NDC	73581023001
Package	100 TABLET in 1 BOTTLE (73581-230-01)
Marketing Start Date	2022-04-15
NDC Exclude Flag	N