NDC 65219-295

Desmopressin Acetate 4 ug per 1 mL injection, solution

On the label: Fresenius Kabi USA, LLC.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Gland Pharma LimitedHyderabad, IndiaMakes it, tests it and packages it Problems found, fixed voluntarilyJun 27, 2023 · 4 inspections

Product details

Generic drug
Desmopressin: every company that makes it
Form
injection, solution, intravenous; subcutaneous
Strength
4 ug per 1 mL
Approval
ANDA ANDA216904
On the market since
Sep 11, 2023
Package NDCs
65219-295-10
Official label
DailyMed (National Library of Medicine), updated Sep 6, 2023

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