Zhejiang Huahai Pharmaceutical Co., Ltd.
Linhai, China · makes it
Serious problems, FDA action Last FDA inspection Apr 24, 2026. 8 inspections on record, 3 with serious problems.
NDC 70518-4567
Escitalopram 10 mg tablet, film coated
On the label: Remedyrepack Inc..
It's a repackaged product: Remedyrepack Inc. rebottles it from BluePoint Laboratories.'s NDC 68001-592.
Where the pills inside were made
Zhejiang Huahai Pharmaceutical Technology Co., Ltd.
Taizhou, China · makes it
Problems found, fixed voluntarily Last FDA inspection Aug 22, 2025. 1 inspection on record.
Product details
- Generic drug
- Escitalopram: see every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 10 mg
- Approval
- ANDA ANDA078032
- On the market since
- Feb 4, 2026
- Package NDCs
70518-4567-0- Official label
- DailyMed (National Library of Medicine), updated Sep 17, 2026
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