Package 0615-8503-39

Brand: loratadine antihistamine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 0615-8503-39
Digits Only 0615850339
Product NDC 0615-8503
Description

30 TABLET in 1 BLISTER PACK (0615-8503-39)

Marketing

Marketing Status
Discontinued 2026-08-31
Brand loratadine antihistamine
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2d41bcf4-af71-4335-8d7c-2d14b5e12706", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311372"], "spl_set_id": ["8d3f03d9-6ae1-46d8-a4f8-c620af029c61"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8503-39)", "package_ndc": "0615-8503-39", "marketing_end_date": "20260831", "marketing_start_date": "20240129"}], "brand_name": "Loratadine antihistamine", "product_id": "0615-8503_2d41bcf4-af71-4335-8d7c-2d14b5e12706", "dosage_form": "TABLET", "product_ndc": "0615-8503", "generic_name": "Loratadine", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine", "brand_name_suffix": "antihistamine", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA076301", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20081015"}