Package 0378-4500-93

Brand: budesonide

Generic: budesonide
NDC Package

Package Facts

Identity

Package NDC 0378-4500-93
Digits Only 0378450093
Product NDC 0378-4500
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4500-93)

Marketing

Marketing Status
Marketed Since 2020-10-21
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": "812acf8d-0936-4ba9-9952-ae9f2266649b", "openfda": {"nui": ["N0000175576", "N0000175450"], "upc": ["0303784500934"], "unii": ["Q3OKS62Q6X"], "rxcui": ["1366550"], "spl_set_id": ["f7265276-e649-4bc4-8ac8-1f5ac2b984e8"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4500-93)", "package_ndc": "0378-4500-93", "marketing_start_date": "20201021"}], "brand_name": "Budesonide", "product_id": "0378-4500_812acf8d-0936-4ba9-9952-ae9f2266649b", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "0378-4500", "generic_name": "Budesonide", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Budesonide", "active_ingredients": [{"name": "BUDESONIDE", "strength": "9 mg/1"}], "application_number": "ANDA208851", "marketing_category": "ANDA", "marketing_start_date": "20201021", "listing_expiration_date": "20261231"}