NDC 0121-0759
Prednisolone Sodium Phosphate 15 mg per 5 mL solution
On the label: Pharmaceutical Associates, Inc..
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 Pharmaceutical Associates, Inc. names for other drugs.
Product details
- Generic drug
- Prednisolone: every company that makes it
- Form
- solution, oral
- Strength
- 15 mg per 5 mL
- Approval
- ANDA ANDA076913
- On the market since
- Apr 25, 2005
- Package NDCs
0121-0759-08- Official label
- DailyMed (National Library of Medicine), updated Jul 10, 2025
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