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Desmopressin acetate

NDC 71288-441 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerMeitheal Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074888
Dosage form / routeINJECTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsDESMOPRESSIN ACETATE (4 ug/mL)
Marketing started20260213
Package count1

External sources

Source: openFDA. Public-domain (CC0).