Package 68682-309-30

Brand: budesonide

Generic: budesonide
NDC Package

Package Facts

Identity

Package NDC 68682-309-30
Digits Only 6868230930
Product NDC 68682-309
Product ID 68682-309_2553124a-3ed4-365d-e063-6294a90a4224
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-309-30)

Marketing

Marketing Status
Marketed Since 2018-07-10
Brand budesonide
Generic budesonide
Sample Package No

Linked Drug Pages (1)

budesonide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2553124a-3ed4-365d-e063-6294a90a4224", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["Q3OKS62Q6X"], "rxcui": ["1366550"], "spl_set_id": ["a12b2e99-c8b3-4d08-9af0-8c4a4376ebf1"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["Oceanside Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-309-30)", "package_ndc": "68682-309-30", "marketing_start_date": "20180710"}], "brand_name": "budesonide", "product_id": "68682-309_2553124a-3ed4-365d-e063-6294a90a4224", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68682-309", "generic_name": "budesonide", "labeler_name": "Oceanside Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "budesonide", "active_ingredients": [{"name": "BUDESONIDE", "strength": "9 mg/1"}], "application_number": "NDA203634", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20180710", "listing_expiration_date": "20261231"}