Sodium Nitroprusside
- Product NDC
- 17478-014
- 11-digit product format
- 174780014
- Labeler code
- 17478
- Product ID
- 17478-014_3a832e69-44fa-4501-9957-5b3b3319b15b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Nitroprusside
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Akorn
- Application
- ANDA208635
- Marketing category
- ANDA
- Marketing start
- 2017-05-04
- Marketing end
- 0000-00-00
- Substance
- SODIUM NITROPRUSSIDE
- Active strength
- 50 mg/2mL
- Pharmacologic classes
- Vasodilation [PE], Vasodilator [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 17478-014-02 | 17478001402 | 1 VIAL, SINGLE-DOSE in 1 CARTON (17478-014-02) > 2 mL in 1 VIAL, SINGLE-DOSE | 2017-05-04 | 0000-00-00 | No | No | Current |