NDC 71839-120

Sodium Nitroprusside 50 mg per 2 mL injection

On the label: BE Pharmaceuticals Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Be Biosol Private LimitedMedchal-Malkajgiri, IndiaMakes it and tests it Problems found, fixed voluntarilyNov 12, 2024 · 3 inspections

Product details

Generic drug
Nitroprusside: every company that makes it
Form
injection, intravenous
Strength
50 mg per 2 mL
Approval
ANDA ANDA214971
On the market since
Jul 12, 2021
Package NDCs
71839-120-01
Official label
DailyMed (National Library of Medicine), updated Jul 22, 2021

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