Sodium Nitroprusside
- Product NDC
- 0548-9401
- 11-digit product format
- 005489401
- Labeler code
- 0548
- Product ID
- 0548-9401_de280771-8cac-4c03-a8c0-cfdbe3d12a0a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sodium Nitroprusside
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Amphastar Pharmaceuticals, Inc.
- Application
- ANDA209832
- Marketing category
- ANDA
- Marketing start
- 2017-12-18
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record