Sodium Nitroprusside
- Product NDC
- 25021-310
- 11-digit product format
- 250210310
- Labeler code
- 25021
- Product ID
- 25021-310_d500db35-05f1-4f03-aeb4-b3b04ef4e300
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Nitroprusside
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA207426
- Marketing category
- ANDA
- Marketing start
- 2016-10-06
- 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
- 2020-12-31
- 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 |
|---|
| 25021-310-02 | 25021031002 | 1 VIAL in 1 CARTON (25021-310-02) > 2 mL in 1 VIAL | 1 vial | 2016-10-06 | 0000-00-00 | No | No | Current |