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
37835-997_35b772eb-9000-2763-e063-6394a90af9d8
Product NDC
37835-997
Form
SPRAY, METERED
Composition / generic term
Fluticasone Propionate
Labeler
Bi-Mart
Marketing category
ANDA
Marketing start / end (source format)
20170517
Source listing expiry
20261231

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 (37835-997-31) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY · 37835-997-31
  • 1 BOTTLE, SPRAY in 1 CARTON (37835-997-44) / 144 SPRAY, METERED in 1 BOTTLE, SPRAY · 37835-997-44

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 →