NDC 70377-129

Sertraline HCl 200 mg capsule

On the label: Biocon Pharma Inc..

Where it's made

Umedica Laboratories Private Limited

Vapi, India · makes it, tests it and packages it

Problems found, fixed voluntarily Last FDA inspection Mar 29, 2024. 4 inspections on record.

Product details

Generic drug
Sertraline: see every company that makes it
Form
capsule, oral
Strength
200 mg
Approval
ANDA ANDA218342
On the market since
Jan 30, 2026
Package NDCs
70377-129-11
Official label
DailyMed (National Library of Medicine), updated Oct 23, 2026

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