Home NDC 16714-015 Desmopressin Acetate
Product NDC 16714-015
11-digit product format 167140015
Labeler code 16714
Product ID 16714-015_a720341d-be60-448e-b39c-05cde487391f
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Desmopressin Acetate
Dosage form INJECTION, SOLUTION
Route INTRAVENOUS; SUBCUTANEOUS
Labeler NorthStar RxLLC
Application ANDA091280
Marketing category ANDA
Marketing start 2020-07-01
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 2021-12-31
Current FDA listing Historical FDA.report record Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 16714-015-01 16714001501 1 VIAL in 1 CARTON (16714-015-01) > 10 mL in 1 VIAL 1 vial 2020-07-01 0000-00-00 No No Current