Vaprisol

Product NDC
0469-1602
11-digit product format
004691602
Labeler code
0469
Product ID
0469-1602_cc0b0c1e-18f6-42cc-8fcb-81fa4e74e5a8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
conivaptan hydrochloride
Dosage form
SOLUTION
Route
INTRAVENOUS
Labeler
Astellas Pharma US, Inc.
Application
NDA021697
Marketing category
NDA
Marketing start
2008-10-08
Marketing end
0000-00-00
Substance
CONIVAPTAN HYDROCHLORIDE
Active strength
20 mg/100mL
Pharmacologic classes
Cytochrome P450 3A Inhibitors [MoA], Vasopressin Receptor Antagonist [EPC], Vasopressin Receptor Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0469-1602-10ML - Milliliter0469-160248f83b90-787a-4139-a2d1-6a018d7c8d8112012-07-24