fluticasone propionate diskus
Generic: fluticasone propionate
Labeler: prasco laboratoriesDrug Facts
Product Profile
Brand Name
fluticasone propionate diskus
Generic Name
fluticasone propionate
Labeler
prasco laboratories
Dosage Form
POWDER, METERED
Routes
Active Ingredients
fluticasone propionate 50 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
66993-790
Product ID
66993-790_6742091b-50f9-4c85-b699-4d1c96b266a6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA020833
Listing Expiration
2026-12-31
Marketing Start
2023-10-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
66993790
Hyphenated Format
66993-790
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
fluticasone propionate diskus (source: ndc)
Generic Name
fluticasone propionate (source: ndc)
Application Number
NDA020833 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/1
Packaging
- 1 INHALER in 1 CARTON (66993-790-97) / 60 POWDER, METERED in 1 INHALER
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["RESPIRATORY (INHALATION)"], "spl_id": "6742091b-50f9-4c85-b699-4d1c96b266a6", "openfda": {"unii": ["O2GMZ0LF5W"], "rxcui": ["896018", "896021", "896025"], "spl_set_id": ["44d009ba-d4b8-410f-b2bc-71ab2d05ac9e"], "manufacturer_name": ["Prasco Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INHALER in 1 CARTON (66993-790-97) / 60 POWDER, METERED in 1 INHALER", "package_ndc": "66993-790-97", "marketing_start_date": "20231030"}], "brand_name": "FLUTICASONE PROPIONATE DISKUS", "product_id": "66993-790_6742091b-50f9-4c85-b699-4d1c96b266a6", "dosage_form": "POWDER, METERED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "66993-790", "generic_name": "fluticasone propionate", "labeler_name": "Prasco Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUTICASONE PROPIONATE", "brand_name_suffix": "DISKUS", "active_ingredients": [{"name": "FLUTICASONE PROPIONATE", "strength": "50 ug/1"}], "application_number": "NDA020833", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20231030", "listing_expiration_date": "20261231"}