FDA NDC Directory · JSON-LD · Markdown

AZELASTINE HYDROCHLORIDE

NDC 68788-8514 · HUMAN PRESCRIPTION DRUG · SPRAY, METERED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA212289
Dosage form / routeSPRAY, METERED · NASAL
Active ingredientsAZELASTINE HYDROCHLORIDE (137 ug/1)
Marketing started20230901
Package count1

External sources

Source: openFDA. Public-domain (CC0).