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DESMOPRESSIN ACETATE

NDC 72843-440 · UBI Pharma Inc.

Generic nameDESMOPRESSIN ACETATE
Dosage formINJECTION
RouteINTRAVENOUS, SUBCUTANEOUS
Active ingredient(s)DESMOPRESSIN ACETATE
Strength40 ug/10mL
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

72843-440-01 — 1 VIAL in 1 CARTON (72843-440-01) / 10 mL in 1 VIAL

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68462-275 — Desmopressin Acetate, 68462-276 — Desmopressin Acetate, 68682-342 — Desmopressin Acetate, 69918-101 — Desmopressin Acetate, 69918-201 — Desmopressin Acetate, 69918-899 — Desmopressin Acetate, 69918-901 — Desmopressin Acetate, 70095-026 — Desmopressin Acetate, 70095-031 — Desmopressin Acetate, 70518-4612 — desmopressin acetate, 71288-440 — Desmopressin acetate, 71288-441 — Desmopressin acetate, 71335-2342 — Desmopressin Acetate, 71863-123 — Desmopressin Acetate Oral Solution, 72485-523 — Desmopressin Acetate, 72485-524 — Desmopressin Acetate, 72843-459 — DESMOPRESSIN ACETATE, 72843-461 — DESMOPRESSIN ACETATE, 83148-126 — Desmopressin Acetate, 83634-451 — 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.