Package 51660-527-31

Brand: allergy relief

Generic: loratadine
NDC Package

Package Facts

Identity

Package NDC 51660-527-31
Digits Only 5166052731
Product NDC 51660-527
Description

30 BLISTER PACK in 1 CARTON (51660-527-31) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2007-08-31
Brand allergy relief
Generic loratadine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7b87d8ea-1102-4642-8a39-b2504dbda716", "openfda": {"unii": ["7AJO3BO7QN"], "rxcui": ["311373"], "spl_set_id": ["de3a7725-5d1b-4195-a9f8-43f92888997c"], "manufacturer_name": ["Ohm Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 CARTON (51660-527-31)  / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "51660-527-31", "marketing_start_date": "20070831"}], "brand_name": "Allergy Relief", "product_id": "51660-527_7b87d8ea-1102-4642-8a39-b2504dbda716", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "51660-527", "generic_name": "Loratadine", "labeler_name": "Ohm Laboratories Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}], "application_number": "ANDA077153", "marketing_category": "ANDA", "marketing_start_date": "20070831", "listing_expiration_date": "20261231"}