NDC 17856-0759
Prednisolone Sodium Phosphate 15 mg per 5 mL solution
On the label: Atlantic Biologicals Corps.. It's repackaged: Atlantic Biologicals Corps. rebottles it from Pharmaceutical Associates, Inc.'s NDC 0121-0759.
Where the pills inside were 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.
Repackaging site
- Atlantic Biologicals Corps, Location not on file · repackages it
Product details
- Generic drug
- Prednisolone: every company that makes it
- Form
- solution
- Strength
- 15 mg per 5 mL
- Approval
- ANDA ANDA076913
- On the market since
- Apr 25, 2005
- Package NDCs
17856-0759-117856-0759-217856-0759-317856-0759-417856-0759-517856-0759-617856-0759-717856-0759-8- Official label
- DailyMed (National Library of Medicine), updated Dec 12, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?