NDC 68999-330
Prednisolone Sodium Phosphate 5 mg per 5 mL solution
On the label: Chartwell Governmental & Specialty RX, 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 Chartwell Governmental & Specialty RX, LLC. names for other drugs.
Product details
- Generic drug
- Prednisolone: every company that makes it
- Form
- solution, oral
- Strength
- 5 mg per 5 mL
- Approval
- ANDA ANDA075988
- On the market since
- May 25, 2004
- Package NDCs
68999-330-0568999-330-24- Official label
- DailyMed (National Library of Medicine), updated Dec 5, 2025
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