Desmopressin Acetate

Product NDC

63629-4816

11-digit product format

636294816

Labeler code

63629

Product ID

63629-4816_33b4f5b2-d4ed-484b-a190-0b148c71a7ef

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Desmopressin Acetate

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA076470

Marketing category

ANDA

Marketing start

2011-08-15

Marketing end

0000-00-00

Substance

DESMOPRESSIN ACETATE

Active strength

0 mg/1

Pharmacologic classes

Factor VIII Activator [EPC],Increased Coagulation Factor VIII Activity [PE],Increased Coagulation Factor VIII Concentration [PE],Vasopressin Analog [EPC],Vasopressins [CS]

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record