United States · FDA National Drug Code directory

AZELASTINE HYDROCHLORIDE AND 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
63629-8612_2cb5fed9-e2fc-448c-87df-83af32f6bc78
Product NDC
63629-8612
Form
SPRAY, METERED
Composition / generic term
azelastine hydrochloride, fluticasone propionate
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20210301
Source listing expiry
20261231

Source-listed ingredients

  • AZELASTINE HYDROCHLORIDE — 137 ug/1
  • FLUTICASONE PROPIONATE — 50 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 BOTTLE in 1 CARTON (63629-8612-1) / 120 SPRAY, METERED in 1 BOTTLE · 63629-8612-1

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 →