Desmopressin Acetate

Product NDC
0115-1647
11-digit product format
001151647
Labeler code
0115
Product ID
0115-1647_d888d0fe-bfd9-4d42-a92c-be4156346491
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Desmopressin Acetate
Dosage form
TABLET
Route
ORAL
Labeler
Impax Generics
Application
ANDA077122
Marketing category
ANDA
Marketing start
2006-01-27
Marketing end
2019-08-31
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
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0115-1647-01EA - Each0115-164784d06f51-8c1b-4197-9d1e-2858f499697a12017-03-06