Desmopressin Acetate

NDC 51655-461 · Northwind Health Company, LLC

Generic nameDesmopressin Acetate

Dosage formTABLET

RouteORAL

Active ingredient(s)DESMOPRESSIN ACETATE

Strength.2 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

51655-461-52 — 30 TABLET in 1 BOTTLE, PLASTIC (51655-461-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

10702-170 — Desmopressin Acetate, 23155-489 — Desmopressin Acetate, 23155-490 — Desmopressin Acetate, 24208-342 — Desmopressin Acetate, 25021-460 — desmopressin acetate, 25021-461 — desmopressin acetate, 39822-6200 — desmopressin acetate, 39822-6250 — desmopressin acetate, 43598-053 — Desmopressin Acetate, 43598-931 — DESMOPRESSIN ACETATE, 55566-2200 — Desmopressin Acetate, 55566-2300 — Desmopressin Acetate, 55566-2600 — Desmopressin Acetate, 55566-2700 — Desmopressin Acetate, 55566-3000 — desmopressin acetate, 59651-249 — desmopressin acetate, 59651-250 — desmopressin acetate, 60505-0257 — desmopressin acetate, 60505-0258 — desmopressin acetate, 60505-0815 — DESMOPRESSIN ACETATE, +34 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.