NDC 70436-028
sodium nitroprusside 50 mg per 2 mL injection, solution, concentrate
On the label: Slate Run Pharmaceuticals, LLC..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Slate Run Pharmaceuticals, LLC. names for other drugs.
Product details
- Generic drug
- Nitroprusside: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 50 mg per 2 mL
- Approval
- ANDA ANDA214199
- On the market since
- Oct 15, 2020
- Package NDCs
70436-028-80- Official label
- DailyMed (National Library of Medicine), updated Oct 15, 2020
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