NDC 0245-0812

Tosymra 10 mg per 0.1 mL spray

On the label: Upsher-Smith Laboratories, LLC.

United States: 1India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
LTS Lakewood, LLCLakewood, NJ, United StatesMakes it and tests it Problems found, fixed voluntarilyJul 29, 2026 · 14 inspections, 1 with FDA action
SMS Pharmaceuticals LimitedHyderabad, IndiaMakes the active ingredient, tests it, packages it and labels it Problems found, fixed voluntarilyMar 21, 2025 · 4 inspections

Product details

Generic drug
Sumatriptan: every company that makes it
Form
spray, nasal
Strength
10 mg per 0.1 mL
Approval
NDA NDA210884
On the market since
Jul 8, 2019
Package NDCs
0245-0812-59 0245-0812-61 0245-0812-89
Official label
DailyMed (National Library of Medicine), updated Nov 18, 2024

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?