Desmopressin Acetate

NDC 69918-101 · Nordic Pharma, Inc.

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 categoryNDA

Packages

69918-101-01 — 1 BOTTLE in 1 CARTON (69918-101-01) / 100 TABLET in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

65145-184 — Desmopressin Acetate, 65219-293 — Desmopressin Acetate, 65219-295 — Desmopressin Acetate, 68001-574 — desmopressin acetate, 68001-575 — desmopressin acetate, 68083-549 — Desmopressin Acetate, 68083-550 — Desmopressin Acetate, 68462-275 — Desmopressin Acetate, 68462-276 — Desmopressin Acetate, 68682-342 — 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, +34 more

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