NDC 72266-141

Azelastine Hydrochloride 0.5 mg per 1 mL solution/ drops

On the label: Fosun Pharma USA Inc..

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Fosun Pharma USA Inc. names for other drugs.

Product details

Generic drug
Azelastine: every company that makes it
Form
solution/ drops, intraocular
Strength
0.5 mg per 1 mL
Approval
ANDA ANDA210092
On the market since
Sep 8, 2020
Package NDCs
72266-141-01
Official label
DailyMed (National Library of Medicine), updated Dec 16, 2025

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