Sodium Nitroprusside
- Product NDC
- 70655-014
- 11-digit product format
- 706550014
- Labeler code
- 70655
- Product ID
- 70655-014_1e7ba4a2-c794-4027-90df-1a73bfb27405
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Nitroprusside
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Renaissance SSA, LLC
- Application
- ANDA209834
- Marketing category
- ANDA
- Marketing start
- 2019-12-28
- 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