Package 0591-2510-30
Brand: budesonide
Generic: budesonidePackage Facts
Identity
Package NDC
0591-2510-30
Digits Only
0591251030
Product NDC
0591-2510
Description
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-2510-30)
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": "5b1c0fe2-b58d-43b4-8784-038653663c44", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0305912510303"], "unii": ["Q3OKS62Q6X"], "rxcui": ["1366550"], "spl_set_id": ["41d4fd39-81ee-41be-b34d-efb12b3a359d"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0591-2510-30)", "package_ndc": "0591-2510-30", "marketing_start_date": "20180705"}], "brand_name": "Budesonide", "product_id": "0591-2510_5b1c0fe2-b58d-43b4-8784-038653663c44", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0591-2510", "generic_name": "Budesonide", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Budesonide", "active_ingredients": [{"name": "BUDESONIDE", "strength": "9 mg/1"}], "application_number": "ANDA205457", "marketing_category": "ANDA", "marketing_start_date": "20180705", "listing_expiration_date": "20261231"}