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
- 0713-0632_0abc4bef-4b22-8a3f-e063-6394a90ae599
- Product NDC
- 0713-0632
- Form
- OINTMENT
- Composition / generic term
- Fluticasone Propionate
- Labeler
- Cosette Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20060531
- Source listing expiry
- 20261231
Source-listed ingredients
- FLUTICASONE PROPIONATE — .05 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 CARTON (0713-0632-15) / 15 g in 1 TUBE · 0713-0632-15
- 1 TUBE in 1 CARTON (0713-0632-31) / 30 g in 1 TUBE · 0713-0632-31
- 1 TUBE in 1 CARTON (0713-0632-60) / 60 g in 1 TUBE · 0713-0632-60
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 →