Package 37808-724-69
Brand: loratadine and pseudoephedrine sulfate
Generic: loratadine and pseudoephedrine sulfatePackage Facts
Identity
Package NDC
37808-724-69
Digits Only
3780872469
Product NDC
37808-724
Description
10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (37808-724-69)
Marketing
Marketing Status
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": "3e9fe73b-d3ee-4160-8dfa-8b099cd68e8a", "openfda": {"unii": ["7AJO3BO7QN", "Y9DL7QPE6B"], "rxcui": ["1117562"], "spl_set_id": ["74e7670a-5eca-4556-a860-0d36e8561518"], "manufacturer_name": ["HEB"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (37808-724-69)", "package_ndc": "37808-724-69", "marketing_start_date": "20180201"}], "brand_name": "Loratadine and Pseudoephedrine Sulfate", "product_id": "37808-724_3e9fe73b-d3ee-4160-8dfa-8b099cd68e8a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "37808-724", "generic_name": "loratadine and pseudoephedrine sulfate", "labeler_name": "HEB", "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": "20180201", "listing_expiration_date": "20261231"}