United States · FDA National Drug Code directory
Nasopro 24
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
- 37808-205_d4e8d5f4-efb9-45e7-b226-c33523a99537
- Product NDC
- 37808-205
- Form
- SPRAY, METERED
- Composition / generic term
- Fluticasone propionate
- Labeler
- H E B
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160530
- 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 (37808-205-08) / 72 SPRAY, METERED in 1 BOTTLE, SPRAY · 37808-205-08
- 1 BOTTLE, SPRAY in 1 CARTON (37808-205-09) / 144 SPRAY, METERED in 1 BOTTLE, SPRAY · 37808-205-09
- 2 BOTTLE, SPRAY in 1 CARTON (37808-205-10) / 144 SPRAY, METERED in 1 BOTTLE, SPRAY · 37808-205-10
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 →