Desmopressin Acetate

Product NDC
0615-7549
11-digit product format
006157549
Labeler code
0615
Product ID
0615-7549_321617aa-3c20-4330-8c8c-7d964d5cab39
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Desmopressin Acetate
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA077122
Marketing category
ANDA
Marketing start
2011-01-17
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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-7549-392021-04-17C16284748780-1960f7f55-c539-8e05-e053-dbdaa90a074a3b937515-0f54-432c-a2bb-793a433719d8
0615-7549-392019-10-29C16284748780-1960f7f55-c539-8e05-e053-dbdaa90a074a3b937515-0f54-432c-a2bb-793a433719d8