SODIUM NITROPRUSSIDE
- Product NDC
- 25208-003
- 11-digit product format
- 252080003
- Labeler code
- 25208
- Product ID
- 25208-003_9e99a701-40c8-4ce1-9f23-b8643678eb92
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SODIUM NITROPRUSSIDE
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Medicure International Inc.
- Application
- ANDA209584
- Marketing category
- ANDA
- Marketing start
- 2018-08-10
- Marketing end
- 0000-00-00
- Substance
- SODIUM NITROPRUSSIDE
- Active strength
- 25 mg/mL
- Pharmacologic classes
- Vasodilation [PE], Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 25208-003-05 | 25208000305 | 1 VIAL, SINGLE-DOSE in 1 CARTON (25208-003-05) > 2 mL in 1 VIAL, SINGLE-DOSE | 2018-08-10 | 0000-00-00 | No | No | Current |