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