United States · FDA National Drug Code directory
Fluticasone Propionate and Salmeterol
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 63629-8810_9e637ba7-f645-48c3-8603-c1bbb0765a65
- Product NDC
- 63629-8810
- Form
- POWDER, METERED
- Composition / generic term
- Fluticasone Propionate and Salmeterol
- Labeler
- Bryant Ranch Prepack
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start / end (source format)
- 20170428
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUTICASONE PROPIONATE — 232 ug/1
- SALMETEROL XINAFOATE — 14 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 POUCH in 1 CARTON (63629-8810-1) / 1 INHALER in 1 POUCH / 60 POWDER, METERED in 1 INHALER · 63629-8810-1
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →