AZELASTINE HYDROCHLORIDE (AZELASTINE HYDROCHLORIDE) — FDA Approval ANDA212775 (AUROBINDO PHARMA LTD)
AZELASTINE HYDROCHLORIDE (AZELASTINE HYDROCHLORIDE) — FDA Approval ANDA212775 (AUROBINDO PHARMA LTD) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: AZELASTINE HYDROCHLORIDE; Active ingredients: AZELASTINE HYDROCHLORIDE; Application number: ANDA212775.
| Brand name | AZELASTINE HYDROCHLORIDE |
|---|---|
| Active ingredients | AZELASTINE HYDROCHLORIDE |
| Application number | ANDA212775 |
| Sponsor | AUROBINDO PHARMA LTD |
| Dosage form | SPRAY, METERED |
| Route | NASAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 20201112 |
| Source | openFDA Drugs@FDA |
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