NDC 51655-461

Desmopressin Acetate 0.2 mg tablet

On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from KVK-TECH, Inc.'s NDC 10702-170.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Kvk-Tech, Inc.Newtown, PA, United StatesMakes it Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action

Repackaging site

Product details

Generic drug
Desmopressin: every company that makes it
Form
tablet, oral
Strength
0.2 mg
Approval
ANDA ANDA210371
On the market since
Oct 29, 2020
Package NDCs
51655-461-52
Official label
DailyMed (National Library of Medicine), updated Jan 1, 2026

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