fluticasone propionate
Generic: fluticasone propionate
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
fluticasone propionate
Generic Name
fluticasone propionate
Labeler
asclemed usa, inc.
Dosage Form
SPRAY, METERED
Routes
Active Ingredients
fluticasone propionate 50 ug/.1g
Manufacturer
Identifiers & Regulatory
Product NDC
76420-106
Product ID
76420-106_ead40f72-3d3e-1c2b-e053-2995a90ad35b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077570
Listing Expiration
2026-12-31
Marketing Start
2008-01-16
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420106
Hyphenated Format
76420-106
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 propionate (source: ndc)
Generic Name
fluticasone propionate (source: ndc)
Application Number
ANDA077570 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/.1g
Packaging
- 16 g in 1 BOTTLE, PUMP (76420-106-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "ead40f72-3d3e-1c2b-e053-2995a90ad35b", "openfda": {"unii": ["O2GMZ0LF5W"], "rxcui": ["1797907"], "spl_set_id": ["75049554-64ca-4efa-b8d1-13cf31d0ff90"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "16 g in 1 BOTTLE, PUMP (76420-106-16)", "package_ndc": "76420-106-16", "marketing_start_date": "20201102"}], "brand_name": "Fluticasone Propionate", "product_id": "76420-106_ead40f72-3d3e-1c2b-e053-2995a90ad35b", "dosage_form": "SPRAY, METERED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "76420-106", "generic_name": "Fluticasone Propionate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluticasone Propionate", "active_ingredients": [{"name": "FLUTICASONE PROPIONATE", "strength": "50 ug/.1g"}], "application_number": "ANDA077570", "marketing_category": "ANDA", "marketing_start_date": "20080116", "listing_expiration_date": "20261231"}