Desmopressin Acetate

Product NDC

0409-2265

11-digit product format

004092265

Labeler code

0409

Product ID

0409-2265_8a765f25-2ddb-45e6-9923-bc73d9da01bb

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Desmopressin Acetate

Dosage form

INJECTION, SOLUTION

Route

INTRAVENOUS; SUBCUTANEOUS

Labeler

Hospira, Inc.

Application

ANDA075220

Marketing category

ANDA

Marketing start

2005-02-28

Marketing end

0000-00-00

Substance

DESMOPRESSIN ACETATE

Active strength

4 ug/mL

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record