fluticasone propionate
Generic: fluticasone propionate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
fluticasone propionate
Generic Name
fluticasone propionate
Labeler
remedyrepack inc.
Dosage Form
SPRAY, METERED
Routes
Active Ingredients
fluticasone propionate 50 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-0880
Product ID
70518-0880_4846e8db-8881-525f-e063-6394a90a7415
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA076504
Listing Expiration
2027-12-31
Marketing Start
2018-03-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705180880
Hyphenated Format
70518-0880
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
ANDA076504 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/1
Packaging
- 1 SPRAY, METERED in 1 CARTON (70518-0880-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["NASAL"], "spl_id": "4846e8db-8881-525f-e063-6394a90a7415", "openfda": {"unii": ["O2GMZ0LF5W"], "rxcui": ["1797907"], "spl_set_id": ["3c7e3ae6-a78f-4023-a2d4-543615ae25b0"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "1 SPRAY, METERED in 1 CARTON (70518-0880-0)", "package_ndc": "70518-0880-0", "marketing_start_date": "20180315"}], "brand_name": "Fluticasone Propionate", "product_id": "70518-0880_4846e8db-8881-525f-e063-6394a90a7415", "dosage_form": "SPRAY, METERED", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-0880", "generic_name": "Fluticasone Propionate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluticasone Propionate", "active_ingredients": [{"name": "FLUTICASONE PROPIONATE", "strength": "50 ug/1"}], "application_number": "ANDA076504", "marketing_category": "ANDA", "marketing_start_date": "20180315", "listing_expiration_date": "20271231"}