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Last Updated: April 28, 2024

Details for New Drug Application (NDA): 213948


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NDA 213948 describes FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE, which is a drug marketed by Hikma and Teva Pharms Usa and is included in two NDAs. It is available from three suppliers. Additional details are available on the FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE profile page.

The generic ingredient in FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE is fluticasone propionate; salmeterol xinafoate. There are twenty-nine drug master file entries for this compound. Twelve suppliers are listed for this compound. Additional details are available on the fluticasone propionate; salmeterol xinafoate profile page.
Pharmacology for NDA: 213948
Suppliers and Packaging for NDA: 213948
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE fluticasone propionate; salmeterol xinafoate POWDER;INHALATION 213948 ANDA Teva Pharmaceuticals USA, Inc. 0093-7516 0093-7516-31 1 POUCH in 1 CARTON (0093-7516-31) / 1 INHALER in 1 POUCH / 60 POWDER in 1 INHALER
FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE fluticasone propionate; salmeterol xinafoate POWDER;INHALATION 213948 ANDA Teva Pharmaceuticals USA, Inc. 0093-7517 0093-7517-31 1 POUCH in 1 CARTON (0093-7517-31) / 1 INHALER in 1 POUCH / 60 POWDER in 1 INHALER

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:POWDER;INHALATIONStrength0.1MG/INH;EQ 0.05MG BASE/INH
Approval Date:Dec 13, 2021TE:ABRLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:POWDER;INHALATIONStrength0.25MG/INH;EQ 0.05MG BASE/INH
Approval Date:Dec 13, 2021TE:ABRLD:No

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:POWDER;INHALATIONStrength0.5MG/INH;EQ 0.05MG BASE/INH
Approval Date:Dec 13, 2021TE:ABRLD:No

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