NDC 71863-123

Desmoda 0.05 mg per 1 mL solution

On the label: Eton Pharmaceuticals, Inc..

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Pharmacia & Upjohn Company LLCKalamazoo, MI, United StatesMakes the active ingredient and tests it Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections
Tulex Pharmaceuticals IncCranbury, NJ, United StatesMakes it and tests it Problems found, fixed voluntarilyMar 24, 2025 · 4 inspections
Eurofins Biopharma Product Testing, Denmark A/SGlostrup, DenmarkTests it No problems foundMay 17, 2023 · 5 inspections
Mikrolab Stockholm ABSollentuna, SwedenTests it Problems found, fixed voluntarilyMar 6, 2025 · 4 inspections
New Jersey LaboratoriesNew Brunswick, NJ, United StatesTests it Problems found, fixed voluntarilySep 22, 2022 · 5 inspections
SGS North America Inc.Lincolnshire, IL, United StatesTests it Problems found, fixed voluntarilyMar 20, 2026 · 9 inspections

Product details

Generic drug
Desmopressin: every company that makes it
Form
solution, oral
Strength
0.05 mg per 1 mL
Approval
NDA NDA219873
On the market since
Mar 2, 2026
Package NDCs
71863-123-14
Official label
DailyMed (National Library of Medicine), updated Mar 2, 2026

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