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
- 68788-8453_2ad7b10a-e9c2-4a64-bea5-f939b62e4f03
- Product NDC
- 68788-8453
- Form
- POWDER
- Composition / generic term
- fluticasone propionate and salmeterol
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230530
- Source listing expiry
- 20261231
Source-listed ingredients
- SALMETEROL XINAFOATE — 50 ug/1
- FLUTICASONE PROPIONATE — 250 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 POUCH in 1 CARTON (68788-8453-6) / 1 INHALER in 1 POUCH / 60 POWDER in 1 INHALER · 68788-8453-6
Source and coverage
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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.
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