Package 72983-503-06

Brand: loratadine

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 72983-503-06
Digits Only 7298350306
Product NDC 72983-503
Description

60 BLISTER PACK in 1 CARTON (72983-503-06) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2024-05-07
Brand loratadine
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "17deb249-05f1-80b0-e063-6294a90a2535", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311373"], "spl_set_id": ["9c168fbb-6668-4a9d-9c7e-d3441e60eb95"], "manufacturer_name": ["Tenshi Kaizen Pvt Ltd"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 BLISTER PACK in 1 CARTON (72983-503-06)  / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "72983-503-06", "marketing_start_date": "20240507"}], "brand_name": "LORATADINE", "product_id": "72983-503_17deb249-05f1-80b0-e063-6294a90a2535", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "72983-503", "generic_name": "LORATADINE", "labeler_name": "Tenshi Kaizen Pvt Ltd", "product_type": "HUMAN OTC DRUG", "brand_name_base": "LORATADINE", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA213294", "marketing_category": "ANDA", "marketing_start_date": "20240507", "listing_expiration_date": "20261231"}