NDC 81033-021
prednisoLONE sodium phosphate 15 mg per 5 mL solution
On the label: Kesin Pharma Corporation.
Where it's made
This label doesn't name the factory that makes the drug (it lists 1 site that packages it and labels it). 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 Kesin Pharma Corporation names for other drugs.
Product details
- Generic drug
- Prednisolone: every company that makes it
- Form
- solution
- Strength
- 15 mg per 5 mL
- Approval
- ANDA ANDA203559
- On the market since
- Oct 27, 2023
- Package NDCs
81033-021-0581033-021-54- Official label
- DailyMed (National Library of Medicine), updated Mar 27, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?