Package 41250-724-69

Brand: loratadine and pseudoephedrine sulfate

Generic: loratadine and pseudoephedrine sulfate
NDC Package

Package Facts

Identity

Package NDC 41250-724-69
Digits Only 4125072469
Product NDC 41250-724
Description

10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (41250-724-69)

Marketing

Marketing Status
Marketed Since 2004-11-17
Brand loratadine and pseudoephedrine sulfate
Generic loratadine and pseudoephedrine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e1ae1d85-8b3c-4a7a-b174-fcb30c3853c8", "openfda": {"unii": ["7AJO3BO7QN", "Y9DL7QPE6B"], "rxcui": ["1117562"], "spl_set_id": ["eb6e2196-2f4f-4fe9-9c80-b4ce89da8db4"], "manufacturer_name": ["Meijer Distribution, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (41250-724-52)", "package_ndc": "41250-724-52", "marketing_start_date": "20041117"}, {"sample": false, "description": "10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (41250-724-69)", "package_ndc": "41250-724-69", "marketing_start_date": "20041117"}], "brand_name": "Loratadine and Pseudoephedrine Sulfate", "product_id": "41250-724_e1ae1d85-8b3c-4a7a-b174-fcb30c3853c8", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "41250-724", "generic_name": "Loratadine and Pseudoephedrine Sulfate", "labeler_name": "Meijer Distribution, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Loratadine and Pseudoephedrine Sulfate", "active_ingredients": [{"name": "LORATADINE", "strength": "10 mg/1"}, {"name": "PSEUDOEPHEDRINE SULFATE", "strength": "240 mg/1"}], "application_number": "ANDA076557", "marketing_category": "ANDA", "marketing_start_date": "20041117", "listing_expiration_date": "20261231"}