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Desmopressin Acetate

NDC 59651-249 · Aurobindo Pharma Limited

Generic namedesmopressin acetate
Dosage formTABLET
RouteORAL
Active ingredient(s)DESMOPRESSIN ACETATE
Strength.1 mg/1
Pharmacologic classFactor VIII Activator [EPC], Increased Coagulation Factor VIII Activity [PE], Increased Coagulation Factor VIII Concentration [PE], Vasopressin Analog [EPC], Vasopressins [CS]
Marketing categoryANDA

Packages

59651-249-01 — 100 TABLET in 1 BOTTLE (59651-249-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

39822-6200 — desmopressin acetate, 39822-6250 — desmopressin acetate, 43598-053 — Desmopressin Acetate, 43598-931 — DESMOPRESSIN ACETATE, 51655-461 — Desmopressin Acetate, 55566-2200 — Desmopressin Acetate, 55566-2300 — Desmopressin Acetate, 55566-2600 — Desmopressin Acetate, 55566-2700 — Desmopressin Acetate, 55566-3000 — desmopressin acetate, 59651-250 — desmopressin acetate, 60505-0257 — desmopressin acetate, 60505-0258 — desmopressin acetate, 60505-0815 — DESMOPRESSIN ACETATE, 60687-721 — desmopressin acetate, 60687-732 — desmopressin acetate, 62756-529 — desmopressin acetate, 63629-3257 — desmopressin acetate, 65145-183 — Desmopressin Acetate, 65145-184 — Desmopressin Acetate, +34 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.