NDC 42799-813
Prednisolone Sodium Phosphate 20 mg per 5 mL solution
On the label: Edenbridge 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 Edenbridge Pharmaceuticals LLC. names for other drugs.
Product details
- Generic drug
- Prednisolone: every company that makes it
- Form
- solution, oral
- Strength
- 20 mg per 5 mL
- Approval
- ANDA ANDA203559
- On the market since
- Nov 11, 2011
- Package NDCs
42799-813-01- Official label
- DailyMed (National Library of Medicine), updated Dec 17, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?