NDC 60687-721 – Desmopressin Acetate

Desmopressin Acetate .1 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC60687-721

Product details

Brand name
Desmopressin Acetate
Generic name
Desmopressin acetate
Labeler
American Health Packaging
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077414
Marketed since
February 16, 2024
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 (1)

Package NDCDescriptionSince
60687-721-2130 BLISTER PACK in 1 CARTON (60687-721-21) / 1 TABLET in 1 BLISTER PACK (60687-721-11)Feb 16, 2024

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