United States · FDA National Drug Code directory
CHILDRENS 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
- 58602-018_0bdbc9dc-56d3-478b-97bc-7e8a43d200b0
- Product NDC
- 58602-018
- Form
- SPRAY, METERED
- Composition / generic term
- fluticasone propionate
- Labeler
- Aurohealth LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240510
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUTICASONE PROPIONATE — 50 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BOTTLE in 1 CARTON (58602-018-04) / 72 SPRAY, METERED in 1 BOTTLE · 58602-018-04
- 1 BOTTLE in 1 CARTON (58602-018-42) / 60 SPRAY, METERED in 1 BOTTLE · 58602-018-42
- 2 BOTTLE in 1 CARTON (58602-018-45) / 72 SPRAY, METERED in 1 BOTTLE · 58602-018-45
- 1 BOTTLE in 1 CARTON (58602-018-51) / 72 SPRAY, METERED in 1 BOTTLE · 58602-018-51
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 →