NDC 71921-170

Sumatriptan 20 mg spray

On the label: Florida Pharmaceutical Products, LLC..

Where it's made

This label doesn't name the factory that makes the drug. 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 Florida Pharmaceutical Products, LLC. names for other drugs.

Product details

Generic drug
Sumatriptan: every company that makes it
Form
spray, nasal
Strength
20 mg
Approval
ANDA ANDA208967
On the market since
May 15, 2021
Package NDCs
71921-170-61
Official label
DailyMed (National Library of Medicine), updated Nov 13, 2021

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