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Desmopressin Acetate

NDC 70095-031 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerSun Pharmaceutical Industries Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA216904
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsDESMOPRESSIN ACETATE (4 ug/mL)
Marketing started20230620
Package count1

External sources

Source: openFDA. Public-domain (CC0).