NDC 23155-489 – Desmopressin Acetate

Desmopressin Acetate .1 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC23155-489

Product details

Brand name
Desmopressin Acetate
Generic name
Desmopressin Acetate
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207880
Marketed since
May 26, 2017
Listing expires
December 31, 2026
Pharmacologic class
Factor VIII Activator; Vasopressin Analog

Active ingredients

Uses, dosage, side effects and warnings for Desmopressin Acetate →

Package NDC codes (2)

Package NDCDescriptionSince
23155-489-01100 TABLET in 1 BOTTLE (23155-489-01)May 26, 2017
23155-489-05500 TABLET in 1 BOTTLE (23155-489-05)May 26, 2017

Recalls mentioning this NDC

Other Desmopressin Acetate products