fluticasone propionate

Generic: fluticasone propionate

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name fluticasone propionate
Generic Name fluticasone propionate
Labeler direct_rx
Dosage Form SPRAY, METERED
Routes
NASAL
Active Ingredients

fluticasone propionate 50 ug/1

Manufacturer
Direct_RX

Identifiers & Regulatory

Product NDC 72189-004
Product ID 72189-004_2c4e8716-fa10-1f1e-e063-6394a90a8a7f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077538
Listing Expiration 2026-12-31
Marketing Start 2019-06-18

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189004
Hyphenated Format 72189-004

Supplemental Identifiers

RxCUI
1797907
UNII
O2GMZ0LF5W

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 ANDA077538 (source: ndc)
Routes
NASAL
source: ndc

Resolved Composition

Strengths
  • 50 ug/1
source: ndc
Packaging
  • 1 SPRAY, METERED in 1 BOTTLE, SPRAY (72189-004-01)
source: ndc

Packages (1)

Ingredients (1)

fluticasone propionate (50 ug/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "2c4e8716-fa10-1f1e-e063-6394a90a8a7f", "openfda": {"unii": ["O2GMZ0LF5W"], "rxcui": ["1797907"], "spl_set_id": ["8b9f7474-8d89-b3e6-e053-2995a90aeddb"], "manufacturer_name": ["Direct_RX"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SPRAY, METERED in 1 BOTTLE, SPRAY (72189-004-01)", "package_ndc": "72189-004-01", "marketing_start_date": "20190618"}], "brand_name": "Fluticasone Propionate", "product_id": "72189-004_2c4e8716-fa10-1f1e-e063-6394a90a8a7f", "dosage_form": "SPRAY, METERED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72189-004", "generic_name": "Fluticasone Propionate", "labeler_name": "Direct_RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluticasone Propionate", "active_ingredients": [{"name": "FLUTICASONE PROPIONATE", "strength": "50 ug/1"}], "application_number": "ANDA077538", "marketing_category": "ANDA", "marketing_start_date": "20190618", "listing_expiration_date": "20261231"}