United States · FDA National Drug Code directory

Fluticasone Propionate

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
0363-0652_2444f8c4-4ebd-4030-a51c-b778ce905b1d
Product NDC
0363-0652
Form
SPRAY, METERED
Composition / generic term
Fluticasone Propionate
Labeler
Walgreens
Marketing category
ANDA
Marketing start / end (source format)
20250701
Source listing expiry
20271231

Source-listed ingredients

  • FLUTICASONE PROPIONATE — 50 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE, SPRAY in 1 CARTON (0363-0652-01) / 144 SPRAY, METERED in 1 BOTTLE, SPRAY (0363-0652-04) · 0363-0652-01
  • 2 BOTTLE, SPRAY in 1 CARTON (0363-0652-02) / 144 SPRAY, METERED in 1 BOTTLE, SPRAY · 0363-0652-02
  • 1 BOTTLE, SPRAY in 1 CARTON (0363-0652-03) / 72 SPRAY, METERED in 1 BOTTLE, SPRAY (0363-0652-05) · 0363-0652-03
  • 4 BOTTLE, SPRAY in 1 CARTON (0363-0652-06) / 144 SPRAY, METERED in 1 BOTTLE, SPRAY · 0363-0652-06

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 →