budesonide
Generic: budesonide
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
budesonide
Generic Name
budesonide
Labeler
a-s medication solutions
Dosage Form
SUSPENSION
Routes
Active Ingredients
budesonide .25 mg/2mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-1467
Product ID
50090-1467_ab2faae8-3e28-451b-b901-a9b24fe0e104
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077519
Listing Expiration
2026-12-31
Marketing Start
2008-11-19
Pharmacologic Class
Established (EPC)
Mechanism of Action
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500901467
Hyphenated Format
50090-1467
Supplemental Identifiers
RxCUI
UNII
NUI
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
budesonide (source: ndc)
Generic Name
budesonide (source: ndc)
Application Number
ANDA077519 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .25 mg/2mL
Packaging
- 30 VIAL in 1 CARTON (50090-1467-0) / 2 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "ab2faae8-3e28-451b-b901-a9b24fe0e104", "openfda": {"nui": ["N0000175576", "N0000175450"], "unii": ["Q3OKS62Q6X"], "rxcui": ["349094"], "spl_set_id": ["32e30f11-e19b-4e23-a893-92d95e48edef"], "pharm_class_epc": ["Corticosteroid [EPC]"], "pharm_class_moa": ["Corticosteroid Hormone Receptor Agonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 VIAL in 1 CARTON (50090-1467-0) / 2 mL in 1 VIAL", "package_ndc": "50090-1467-0", "marketing_start_date": "20141128"}], "brand_name": "Budesonide", "product_id": "50090-1467_ab2faae8-3e28-451b-b901-a9b24fe0e104", "dosage_form": "SUSPENSION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-1467", "generic_name": "Budesonide", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Budesonide", "active_ingredients": [{"name": "BUDESONIDE", "strength": ".25 mg/2mL"}], "application_number": "ANDA077519", "marketing_category": "ANDA", "marketing_start_date": "20081119", "listing_expiration_date": "20261231"}