NDC 69097-451

Sertraline Hydrochloride 200 mg capsule

On the label: Cipla USA., Inc..

Where it's made

Zenara Pharma Private Limited

Hyderabad, India · makes it, tests it, packages it and labels it

Problems found, fixed voluntarily Last FDA inspection May 21, 2024. 1 inspection on record.

Product details

Generic drug
Sertraline: see every company that makes it
Form
capsule, oral
Strength
200 mg
Approval
ANDA ANDA218853
On the market since
Jul 17, 2025
Package NDCs
69097-451-02
Official label
DailyMed (National Library of Medicine), updated Jul 16, 2025

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