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LORATADINE TAB 10 MG 300 CT

Generic: Loratadine

NDC:70010-0162-34

Manufacturer:Granules Pharmaceuticals Inc.

Strength:10 mg/1

Dosage Form:TABLET

Route:ORAL

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Drug Information

Identification

Generic Name

Loratadine

Brand Name

Loratadine

Labeler / Distributor

Granules Pharmaceuticals Inc.

Product Type

HUMAN OTC DRUG

Administration

Dosage Form

TABLET

Route of Administration

ORAL

FDA Application Number

ANDA210722

Active Ingredients

Ingredient	Strength
LORATADINE	10 mg/1

Data sourced from openFDA / DailyMed. For full prescribing information, consult the drug label.

Wholesale compliance resources

DSCSA T2 documents DSCSA compliance resource hub

Drug Resources

Loratadine Drug Page NDC 70010-0162-34 Lookup

Clinical Drug Information

Indications & Usage

USE(S) temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:  runny nose  sneezing  itchy, water eyes  itching of the nose or throat

Warnings

WARNINGS DO NOT USE if you have ever had an allergic reaction to this product or any of its ingredients

Dosage & Administration

DIRECTIONS adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor

Clinical data sourced from openFDA drug labeling. For complete prescribing information, consult the full drug label.