NDC 53002-1803
Azelastine Hydrochloride 0.5 mg per 1 mL solution/ drops
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Sandoz Inc.'s NDC 61314-308.
Where the pills inside were 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 Sandoz Inc. names for other drugs.
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · relabels it
Product details
- Generic drug
- Azelastine: every company that makes it
- Form
- solution/ drops
- Strength
- 0.5 mg per 1 mL
- Approval
- ANDA ANDA202305
- On the market since
- Mar 21, 2013
- Package NDCs
53002-1803-1- Official label
- DailyMed (National Library of Medicine), updated Jun 6, 2023
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