Package 53746-778-10
Brand: budesonide
Generic: budesonidePackage Facts
Identity
Package NDC
53746-778-10
Digits Only
5374677810
Product NDC
53746-778
Description
100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (53746-778-10)
Marketing
Marketing Status
Brand
budesonide
Generic
budesonide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6c4112fe-354a-472f-97ba-fa86d405b7f7", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["Q3OKS62Q6X"], "rxcui": ["1244214"], "spl_set_id": ["10336e42-0e9d-45c4-80bc-5149d5ec9e1c"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Amneal Pharmaceuticals of New York LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (53746-778-10)", "package_ndc": "53746-778-10", "marketing_start_date": "20250522"}], "brand_name": "Budesonide", "product_id": "53746-778_6c4112fe-354a-472f-97ba-fa86d405b7f7", "dosage_form": "CAPSULE, DELAYED RELEASE", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "53746-778", "generic_name": "Budesonide", "labeler_name": "Amneal Pharmaceuticals of New York LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Budesonide", "active_ingredients": [{"name": "BUDESONIDE", "strength": "3 mg/1"}], "application_number": "ANDA206200", "marketing_category": "ANDA", "marketing_start_date": "20250522", "listing_expiration_date": "20261231"}