NDC 53002-0510
Olopatadine Hydrochloride 1.11 mg per 1 mL solution/ drops
On the label: RPK Pharmaceuticals, Inc.. It's repackaged from NDC 70069-007, made by Somerset Therapeutics, LLC (Olopatadine Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it and relabels it). 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 RPK Pharmaceuticals, Inc. names for other drugs.
Product details
- Generic drug
- Olopatadine: every company that makes it
- Form
- solution/ drops
- Strength
- 1.11 mg per 1 mL
- Approval
- ANDA ANDA206306
- On the market since
- Dec 7, 2015
- Package NDCs
53002-0510-1- Official label
- DailyMed (National Library of Medicine), updated Jun 7, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?