NDC 66993-135

Fluticasone Furoate and Vilanterol

Fluticasone Furoate And Vilanterol

Fluticasone Furoate and Vilanterol is a Respiratory (inhalation) Powder in the Human Prescription Drug category. It is labeled and distributed by Prasco Laboratories. The primary component is Fluticasone Furoate; Vilanterol Trifenatate.

• Product ID: 66993-135_b7c053e6-82c4-49be-9331-1edcb64439ca
• NDC: 66993-135
• Product Type: Human Prescription Drug
• Proprietary Name: Fluticasone Furoate and Vilanterol
• Generic Name: Fluticasone Furoate And Vilanterol
• Dosage Form: Powder
• Route of Administration: RESPIRATORY (INHALATION)
• Marketing Start Date: 2022-05-23
• Marketing Category: NDA AUTHORIZED GENERIC /
• Application Number: NDA204275
• Labeler Name: Prasco Laboratories
• Substance Name: FLUTICASONE FUROATE; VILANTEROL TRIFENATATE
• Active Ingredient Strength: 100 ug/1; ug/1
• Pharm Classes: Adrenergic beta2-Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], beta2-Adrenergic Agonist [EPC]
• NDC Exclude Flag: N
• Listing Certified Through: 2023-12-31

Packaging

NDC 66993-135-97

1 TRAY in 1 CARTON (66993-135-97) > 1 INHALER in 1 TRAY > 30 POWDER in 1 INHALER

• Marketing Start Date: 2022-05-23
• NDC Exclude Flag: N
• Sample Package?: N

Drug Details

NDC Crossover Matching brand name "Fluticasone Furoate and Vilanterol" or generic name "Fluticasone Furoate And Vilanterol"

NDC	Brand Name	Generic Name
66993-135	Fluticasone Furoate and Vilanterol	fluticasone furoate and vilanterol
66993-136	Fluticasone Furoate and Vilanterol	fluticasone furoate and vilanterol