NDC 71335-2317

Furosemide 40 mg tablet

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Rising Pharma Holdings, Inc.'s NDC 64980-563.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Graviti Pharmaceuticals Private LimitedSangareddy, IndiaMakes it and tests it Problems found, fixed voluntarilyJul 28, 2026 · 2 inspections

Repackaging site

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Furosemide: every company that makes it
Form
tablet, oral
Strength
40 mg
Approval
ANDA ANDA216629
On the market since
Nov 5, 2022
Package NDCs
71335-2317-1 71335-2317-2 71335-2317-3 71335-2317-4 71335-2317-5 71335-2317-6 71335-2317-7 71335-2317-8 71335-2317-9
Official label
DailyMed (National Library of Medicine), updated Jan 2, 2024

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