fluticasone
Generic: fluticasone propionate
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
fluticasone
Generic Name
fluticasone propionate
Labeler
preferred pharmaceuticals inc.
Dosage Form
SPRAY, METERED
Routes
Active Ingredients
fluticasone propionate 50 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-7788
Product ID
68788-7788_1b74a3c8-4827-440d-aaf0-950b2d0a4966
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078492
Listing Expiration
2026-12-31
Marketing Start
2020-10-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687887788
Hyphenated Format
68788-7788
Supplemental Identifiers
RxCUI
UNII
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 (source: ndc)
Generic Name
fluticasone propionate (source: ndc)
Application Number
ANDA078492 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/1
Packaging
- 1 BOTTLE, SPRAY in 1 BOX (68788-7788-1) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "1b74a3c8-4827-440d-aaf0-950b2d0a4966", "openfda": {"unii": ["O2GMZ0LF5W"], "rxcui": ["1797907"], "spl_set_id": ["29e9f228-ee69-4d26-b5db-81b2fd5f1bee"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, SPRAY in 1 BOX (68788-7788-1) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY", "package_ndc": "68788-7788-1", "marketing_start_date": "20201021"}], "brand_name": "FLUTICASONE", "product_id": "68788-7788_1b74a3c8-4827-440d-aaf0-950b2d0a4966", "dosage_form": "SPRAY, METERED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "68788-7788", "generic_name": "fluticasone propionate", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUTICASONE", "active_ingredients": [{"name": "FLUTICASONE PROPIONATE", "strength": "50 ug/1"}], "application_number": "ANDA078492", "marketing_category": "ANDA", "marketing_start_date": "20201021", "listing_expiration_date": "20261231"}